Toolkit Items

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.

3 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.

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light-controlled subcellular recruitment

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cytoplasmically diffuse CRY2 and membrane-anchored CIBN

Multi-Component Switch

Cytoplasmically diffuse CRY2 with membrane-anchored CIBN is a proof-of-concept CRY2/CIB optogenetic configuration adapted into Drosophila-oriented vector systems. It was proposed to use blue light to recruit CRY2 fusion proteins, including a possible CRY2-Rho1 fusion, to the plasma membrane.

CFBacMamMusHumTxRep
Ev 28Rep 9Pr 71

CRY2/CIB system

Multi-Component Switch

The CRY2/CIB system is a blue-light-responsive optogenetic multi-component switch used for gene regulation and control of protein recruitment. The supplied evidence identifies it as a well-known optogenetic system and indicates that blue light can recruit CRY2-fused cargo to membrane-anchored CIB for spatial and temporal control of downstream cellular events.

CFBacMamMusHumTxRep
Ev 28Rep 9Pr 37

Rho1-CRY2 fusion construct

Multi-Component Switch

The Rho1-CRY2 fusion construct is a proposed optogenetic multi-component switch for Drosophila in which a small G protein Rho variant would be fused to CRY2. The intended function is blue-light-dependent recruitment of Rho1-CRY2 to membrane-anchored CIB to control subcellular localization and downstream events, but the available evidence indicates the construct was still being cloned rather than functionally validated.

CFBacMamMusHumTxRep
Ev 28Rep 9Pr 37
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