活细胞中的 G 蛋白偶联受体信号复合体。

Cellular logistics Pub Date : 2014-06-04 eCollection Date: 2014-01-01 DOI:10.4161/cl.29392
John R Hepler
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引用次数: 0

摘要

基于生化研究的受体(GPCR)和 G 蛋白(Gαβγ)信号传导经典模型提出,受体刺激导致 G 蛋白活化(Gα-GTP)和异源三聚体(Gα-GTP + Gβγ)解离,从而调节下游信号传导事件。目前尚不清楚细胞膜上是否存在可自由扩散的活化 Gα-GTP,能够催化信号放大。最近在活细胞中进行的研究表明,GPCR 是组装大分子信号复合体的平台,其中包括支持高效和空间受限信号事件的 G 蛋白,而不需要 Gα-GTP 和 Gβγ 在质膜内完全解离和横向扩散。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
G protein coupled receptor signaling complexes in live cells.

Classical models of receptor (GPCR) and G protein (Gαβγ) signaling based on biochemical studies have proposed that receptor stimulation results in G protein activation (Gα-GTP) and dissociation of the heterotrimer (Gα-GTP + Gβγ) to regulate downstream signaling events. Unclear is whether or not there exists freely diffusible, activated Gα-GTP on cellular membranes capable of catalytic signal amplification. Recent studies in live cells indicate that GPCRs serve as platforms for the assembly of macromolecular signaling complexes that include G proteins to support a highly efficient and spatially restricted signaling event, with no requirement for full Gα-GTP and Gβγ dissociation and lateral diffusion within the plasma membrane.

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