Toolkit/light-activated neurotrophin receptors

light-activated neurotrophin receptors

Multi-Component Switch·Research·Since 2020

Taxonomy: Mechanism Branch / Architecture. Workflows sit above the mechanism and technique branches rather than replacing them.

Summary

Light-activated neurotrophin receptors are engineered optogenetic multi-component receptor systems built using the improved light-induced dimerizer (iLID). The available evidence indicates that they use light-controlled iLID interactions to drive neurotrophin receptor assembly or activation.

Usefulness & Problems

Why this is useful

These systems are useful as optogenetic tools for controlling neurotrophin receptor signaling with light. The supplied evidence supports their relevance for constructing light-responsive receptor assemblies, but does not provide detailed application data or performance benchmarks.

Problem solved

They address the problem of making neurotrophin receptor activity controllable by light through an engineered iLID-based design. The evidence does not further specify which experimental limitations of conventional neurotrophin stimulation were tested or overcome.

Problem links

Need precise spatiotemporal control with light input

Derived

Light-activated neurotrophin receptors are engineered multi-component optogenetic receptor systems constructed using the improved light-induced dimerizer (iLID). The available evidence indicates that these tools use light to control neurotrophin receptor assembly or activation through iLID-based interactions.

Taxonomy & Function

Primary hierarchy

Mechanism Branch

Architecture: A composed arrangement of multiple parts that instantiates one or more mechanisms.

Techniques

No technique tags yet.

Target processes

No target processes tagged yet.

Input: Light

Implementation Constraints

cofactor dependency: cofactor requirement unknownencoding mode: genetically encodedimplementation constraint: context specific validationimplementation constraint: multi component delivery burdenimplementation constraint: spectral hardware requirementoperating role: actuatorswitch architecture: multi componentswitch architecture: recruitment

Implementation is based on iLID, implying a multi-component construct architecture that uses engineered light-induced interactions. The supplied evidence supports domain-fusion-style construction but does not provide construct maps, expression context, cofactors, or delivery details.

The evidence is very limited and only establishes that the tool class was constructed using iLID. It does not specify receptor subtype, illumination wavelength, activation efficiency, downstream signaling outputs, or independent validation.

Validation

Cell-freeBacteriaMammalianMouseHumanTherapeuticIndep. Replication

Supporting Sources

Ranked Claims

Claim 1review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 2review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 3review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 4review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 5review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 6review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 7review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 8review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 9review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 10review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 11review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 12review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 13review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 14review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 15review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 16review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 17review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 18review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 19review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 20review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 21review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 22review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 23review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 24review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 25review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 26review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Claim 27review scopesupports2020Source 1needs review

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Approval Evidence

1 source1 linked approval claimfirst-pass slug light-activated-neurotrophin-receptors
Construction of Light-Activated Neurotrophin Receptors Using the Improved Light-Induced Dimerizer (iLID)

Source:

review scopesupports

This review concerns the construction of light-activated neurotrophin receptors using iLID.

Source:

Comparisons

Source-backed strengths

A clear strength is that these receptors are explicitly constructed as light-activated systems using the improved light-induced dimerizer, supporting optical control over receptor behavior. Beyond this construction-level claim, the provided evidence does not report quantitative strengths such as kinetics, dynamic range, reversibility, or cellular validation breadth.

Compared with LightOn system

light-activated neurotrophin receptors and LightOn system address a similar problem space.

Shared frame: same top-level item type; shared mechanisms: heterodimerization; same primary input modality: light

light-activated neurotrophin receptors and photo-activatable Akt probe address a similar problem space.

Shared frame: same top-level item type; shared mechanisms: heterodimerization; same primary input modality: light

light-activated neurotrophin receptors and tandem-dimer nano (tdnano) address a similar problem space.

Shared frame: same top-level item type; shared mechanisms: heterodimerization; same primary input modality: light

Ranked Citations

  1. 1.
    StructuralSource 1Journal of Molecular Biology2020Claim 22Claim 21Claim 21

    Seeded from load plan for claim c1. Extracted from this source document.