Toolkit/Gβγ-sequestering domain

Gβγ-sequestering domain

Protein Domain·Research·Since 2014

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

Summary

The Gβγ-sequestering domain is a protein domain used in an optogenetic configuration to inhibit G protein signaling at selected plasma membrane regions. In the cited study, light-triggered recruitment of this domain to the plasma membrane produced localized suppression of G protein signaling.

Usefulness & Problems

Why this is useful

This domain is useful for spatially restricting inhibition of G protein signaling rather than perturbing signaling globally. The available evidence supports its use for generating subcellularly localized signaling perturbations at the plasma membrane.

Problem solved

It addresses the problem of inhibiting G protein signaling with subcellular precision. Specifically, light-triggered membrane recruitment enables localized suppression of signaling in a chosen plasma membrane region.

Taxonomy & Function

Primary hierarchy

Mechanism Branch

Component: A low-level protein part used inside a larger architecture that realizes a mechanism.

Techniques

No technique tags yet.

Target processes

localizationsignaling

Input: Light

Implementation Constraints

The available evidence indicates that the domain was used in an optogenetic recruitment setup in which light triggers its localization to a selected plasma membrane region. No further practical details are provided here regarding construct architecture, fusion partners, illumination wavelength, cofactors, or expression system.

The supplied evidence is limited to a single statement from one study and does not define the domain sequence, binding specificity, kinetics, reversibility, or magnitude of inhibition. It also does not establish performance across multiple cell types, organisms, or signaling contexts.

Validation

Cell-freeBacteriaMammalianMouseHumanTherapeuticIndep. Replication

Supporting Sources

Ranked Claims

Claim 1mechanism of actionsupports2014Source 1needs review

Light-triggered recruitment of a truncated RGS protein or a Gβγ-sequestering domain to a selected plasma membrane region causes localized inhibition of G protein signaling.

Light-triggered recruitment of a truncated regulator of G protein signaling (RGS) protein or a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.
Claim 2mechanism of actionsupports2014Source 1needs review

Light-triggered recruitment of a truncated RGS protein or a Gβγ-sequestering domain to a selected plasma membrane region causes localized inhibition of G protein signaling.

Light-triggered recruitment of a truncated regulator of G protein signaling (RGS) protein or a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.
Claim 3mechanism of actionsupports2014Source 1needs review

Light-triggered recruitment of a truncated RGS protein or a Gβγ-sequestering domain to a selected plasma membrane region causes localized inhibition of G protein signaling.

Light-triggered recruitment of a truncated regulator of G protein signaling (RGS) protein or a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.
Claim 4mechanism of actionsupports2014Source 1needs review

Light-triggered recruitment of a truncated RGS protein or a Gβγ-sequestering domain to a selected plasma membrane region causes localized inhibition of G protein signaling.

Light-triggered recruitment of a truncated regulator of G protein signaling (RGS) protein or a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.
Claim 5mechanism of actionsupports2014Source 1needs review

Light-triggered recruitment of a truncated RGS protein or a Gβγ-sequestering domain to a selected plasma membrane region causes localized inhibition of G protein signaling.

Light-triggered recruitment of a truncated regulator of G protein signaling (RGS) protein or a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.
Claim 6mechanism of actionsupports2014Source 1needs review

Light-triggered recruitment of a truncated RGS protein or a Gβγ-sequestering domain to a selected plasma membrane region causes localized inhibition of G protein signaling.

Light-triggered recruitment of a truncated regulator of G protein signaling (RGS) protein or a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.
Claim 7mechanism of actionsupports2014Source 1needs review

Light-triggered recruitment of a truncated RGS protein or a Gβγ-sequestering domain to a selected plasma membrane region causes localized inhibition of G protein signaling.

Light-triggered recruitment of a truncated regulator of G protein signaling (RGS) protein or a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.

Approval Evidence

1 source1 linked approval claimfirst-pass slug g-sequestering-domain
Light-triggered recruitment of ... a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.

Source:

mechanism of actionsupports

Light-triggered recruitment of a truncated RGS protein or a Gβγ-sequestering domain to a selected plasma membrane region causes localized inhibition of G protein signaling.

Light-triggered recruitment of a truncated regulator of G protein signaling (RGS) protein or a Gβγ-sequestering domain to a selected region on the plasma membrane results in localized inhibition of G protein signaling.

Source:

Comparisons

Source-backed strengths

The reported strength is spatially localized inhibition of G protein signaling following light-triggered recruitment to the plasma membrane. The evidence directly supports subcellular control of signaling inhibition, but does not provide quantitative performance metrics in the supplied material.

Ranked Citations

  1. 1.
    StructuralSource 1Molecular Biology of the Cell2014Claim 1Claim 2Claim 3

    Extracted from this source document.