BcLOVclust

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

BcLOVclust can be applied to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

Source: Rapid Optogenetic Clustering in the Cytoplasm with BcLOVclust.

BcLOVclust shows substantially faster clustering and de-clustering kinetics than Cry2.

This variant-called BcLOVclust-clustered over many cycles with substantially faster clustering and de-clustering kinetics compared to the widely used optogenetic clustering protein Cry2.

Source: Rapid Optogenetic Clustering in the Cytoplasm with BcLOVclust.

BcLOVclust is an engineered BcLOV4-derived variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Herein we identify key amino acids that couple BcLOV4 clustering to membrane binding, allowing us to engineer a variant that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

Source: Rapid Optogenetic Clustering in the Cytoplasm with BcLOVclust.

BcLOVclust is temperature sensitive, and its light-induced clusters dissolve faster at higher temperature despite constant illumination.

Like wt BcLOV4, BcLOVclust activity was sensitive to temperature: light-induced clusters spontaneously dissolved at a rate that increased with temperature despite constant illumination.

Source: Rapid Optogenetic Clustering in the Cytoplasm with BcLOVclust.

BcLOVclust clustering magnitude can be strengthened by appending a FUS intrinsically disordered region or by selecting the fused fluorescent protein.

The magnitude of clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by selecting the appropriate fluorescent protein to which it was fused.

Source: Rapid Optogenetic Clustering in the Cytoplasm with BcLOVclust.

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to control independent protein condensates with light.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

Source: Rapid Optogenetic Clustering in the Cytoplasm with BcLOVclust.

BcLOVclust is currently best suited for cells and organisms cultured below approximately 30 °C rather than physiological mammalian temperatures.

While its usage is currently best suited in cells and organisms that can be cultured below ∼30 °C, a deeper understanding of BcLOVclust thermal response will further enable its use at physiological mammalian temperatures.

Source: Rapid Optogenetic Clustering in the Cytoplasm with BcLOVclust.

Current use of BcLOVclust is suited for organisms that can be cultured below approximately 30 degrees Celsius.

While its usage is currently suited for organisms that can be cultured below ∼30 °C

Source: Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant

BcLOVclust can be used to control signaling proteins and stress granules in mammalian cells.

BcLOVclust could also be applied to control signaling proteins and stress granules in mammalian cells.

Source: Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant

BcLOVclust has dramatically faster clustering and de-clustering kinetics than Cry2.

BcLOVclust, clustered over many cycles with dramatically faster clustering and de-clustering kinetics compared to Cry2

Source: Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant

A BcLOV4 variant was engineered that clusters in the cytoplasm and does not associate with the membrane in response to blue light.

allowing us to engineer a variant of BcLOV4 that clusters in the cytoplasm and does not associate with the membrane in response to blue light

Source: Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant

BcLOVclust clustering magnitude can be increased by appending a FUS intrinsically disordered region or by optimizing the fused fluorescent protein.

The magnitude of BcLOVclust clustering could be strengthened by appending an intrinsically disordered region from the fused in sarcoma (FUS) protein, or by optimizing the fluorescent protein to which it was fused.

Source: Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant

At low temperatures, BcLOVclust and Cry2 can be multiplexed in the same cells to independently control protein condensates.

At low temperatures, BcLOVclust and Cry2 could be multiplexed in the same cells, allowing light control of independent protein condensates.

Source: Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant

BcLOVclust retains temperature sensitivity such that light-induced clustering is transient and spontaneous declustering increases with temperature.

BcLOVclust retained the temperature sensitivity of BcLOV4 such that light induced clustering was transient, and the rate of spontaneous declustering increased with temperature.

Source: Rapid optogenetic clustering of a cytoplasmic BcLOV4 variant