LiGluR
Multi-Component SwitchThe supplied web research summary lists LiGluR as an explicitly supported related tool/component connected to the review's focus on optical control of neuronal receptors.
Browse the toolkit beneath workflows. The mechanism branch runs mechanism -> architecture -> component, while the technique branch runs from high-level approaches down to concrete methods.
5 items matching 1 filter
Mechanism Branch
Layer 1
Mechanisms
Top-level concepts: biophysical action modes such as heterodimerization, photocleavage, or RNA binding.
Layer 2
Architectures
Arrangements that realize or deploy mechanisms, including switches, construct patterns, and delivery strategies.
Layer 3
Components
Low-level parts and sequence-defined elements used inside architectures, including protein domains and RNA elements.
Technique Branch
Layer 1
Approaches
High-level engineering practices such as computational design, directed evolution, sequence verification, and functional assay.
Layer 2
Methods
Concrete methods used to design, build, verify, or characterize engineered systems.
Showing 1-5 of 5
The supplied web research summary lists LiGluR as an explicitly supported related tool/component connected to the review's focus on optical control of neuronal receptors.
One such PTL, maleimide-azobenzene-quaternary ammonium (MAQ), contains a maleimide (M) to tether the molecule to a genetically engineered cysteine, a photoisomerizable azobenzene (A) linker and a pore-blocking quaternary ammonium group (Q).
The NaYF4:Yb/Tm/Er upconversion nanoparticle is a light-responsive siRNA delivery nanocarrier reported for near-infrared-controlled gene silencing. In the described system, NaYF4:Yb/Tm/Er upconversion converts NIR irradiation into UV emission that induces azobenzene photoisomerization and triggers controlled siRNA release.
MAQ was originally used to photocontrol SPARK, an engineered light-gated potassium channel derived from Shaker.
The upconversion nanoparticle-based siRNA nanocarrier is a nanoparticle delivery system reported to enable near-infrared-induced, spatiotemporally controlled gene silencing. It was demonstrated for spatially restricted GFP knockdown in 2D cell culture and 3D multicellular tumor spheroids.