fluorescein-based SynNotch adaptors
Construct PatternHere, we introduce an adaptor-based strategy for regulating SynNotch activity via fluorescein isomers and analogs.
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.
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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
Here, we introduce an adaptor-based strategy for regulating SynNotch activity via fluorescein isomers and analogs.
fluorescein-conjugated extracellular matrix (ECM)-binding peptides can be used to regulate SynNotch activity depending on the folding state of collagen-based ECM networks
The web research summary states that the anchor paper describes MRS7145 as the first light-dependent adenosine A2A receptor antagonist and identifies it as the photo-controlled/photocaged adenosine A2A receptor antagonist used for light-dependent blockade in cells and behaving animals.
we demonstrate the feasibility and experimental advantages of in vivo photopharmacology using "caged" opioid drugs that are activated in the brain with light after systemic administration in an inactive form
Using an optimized fluorescein-binding SynNotch receptor, we describe ways to chemically control SynNotch signaling...