Toolkit/engineered chimeric receptors

engineered chimeric receptors

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

Summary

Engineered chimeric receptors are described as an opsin-related optical tool class for manipulating neuromodulatory GPCR signaling. They imply receptor constructs that couple light input to GPCR pathway control.

Usefulness & Problems

No literature-backed usefulness or problem-fit explainer has been materialized for this record yet.

Taxonomy & Function

Primary hierarchy

Mechanism Branch

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

Target processes

recombinationsignaling

Input: Light

Validation

Cell-freeBacteriaMammalianMouseHumanTherapeuticIndep. Replication

Supporting Sources

Ranked Claims

Claim 1application scopesupports2016Source 1needs review

These optical techniques targeting specific members of the GPCR signaling pathway provide a broad base for investigating GPCR signaling in behavior and disease states and may support therapeutic development.

These emerging techniques targeting specific members of the GPCR signaling pathway offer an expansive base for investigating GPCR signaling in behavior and disease states, in addition to paving a path to potential therapeutic developments.
Claim 2capability summarysupports2016Source 1needs review

Optogenetics provides means to control cell signaling with spatiotemporal control in discrete cell types.

Optogenetics has revolutionized neuroscience by providing means to control cell signaling with spatiotemporal control in discrete cell types.
Claim 3deployment summarysupports2016Source 1needs review

Cre-dependent viral vector expression and two-photon microscopy are highlighted as technologies to utilize these optical tools in vitro and in vivo.

we highlight technologies to utilize these tools in vitro and in vivo, including Cre dependent viral vector expression and two-photon microscopy
Claim 4review scope summarysupports2016Source 1needs review

The review organizes optical manipulation of neuromodulatory GPCR signaling into four major tool classes: opsins including engineered chimeric receptors, photoactivatable proteins, photopharmacology using caged or photoswitchable molecules, and fluorescent protein-based reporters and biosensors.

we summarize four major classes of optical tools to manipulate neuromodulatory GPCR signaling: opsins (including engineered chimeric receptors); photoactivatable proteins; photopharmacology through caging-photoswitchable molecules; fluorescent protein based reporters and biosensors

Approval Evidence

1 source3 linked approval claimsfirst-pass slug engineered-chimeric-receptors
opsins (including engineered chimeric receptors)

Source:

application scopesupports

These optical techniques targeting specific members of the GPCR signaling pathway provide a broad base for investigating GPCR signaling in behavior and disease states and may support therapeutic development.

These emerging techniques targeting specific members of the GPCR signaling pathway offer an expansive base for investigating GPCR signaling in behavior and disease states, in addition to paving a path to potential therapeutic developments.

Source:

capability summarysupports

Optogenetics provides means to control cell signaling with spatiotemporal control in discrete cell types.

Optogenetics has revolutionized neuroscience by providing means to control cell signaling with spatiotemporal control in discrete cell types.

Source:

review scope summarysupports

The review organizes optical manipulation of neuromodulatory GPCR signaling into four major tool classes: opsins including engineered chimeric receptors, photoactivatable proteins, photopharmacology using caged or photoswitchable molecules, and fluorescent protein-based reporters and biosensors.

we summarize four major classes of optical tools to manipulate neuromodulatory GPCR signaling: opsins (including engineered chimeric receptors); photoactivatable proteins; photopharmacology through caging-photoswitchable molecules; fluorescent protein based reporters and biosensors

Source:

Comparisons

No literature-backed comparison notes have been materialized for this record yet.

Ranked Citations

  1. 1.
    StructuralSource 1Current Opinion in Pharmacology2016Claim 1Claim 2Claim 3

    Seeded from load plan for claim cl1. Extracted from this source document.