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G蛋白偶联受体(GPCR)配体的信号传导机制。

Signaling mechanisms of GPCR ligands.

作者信息

Strange Philip G

机构信息

School of Pharmacy, University of Reading, PO Box 228, Whiteknights, Reading, RG6 6AJ, UK.

出版信息

Curr Opin Drug Discov Devel. 2008 Mar;11(2):196-202.

Abstract

G protein-coupled receptors constitute one of the major classes of drug targets, so understanding the mechanisms of signaling through these receptors is of great importance. This review covers some of the recent advances in G protein-coupled receptor signaling. A high resolution structure of the beta 2-adrenergic receptor has been reported, as well as several molecular switches involved in receptor activation. It has also been realised that receptors and G proteins and their subunits may not always separate upon receptor activation. The definition of the ability of these receptors to signal has been expanded considerably with the realisation that some signaling may occur independently of G proteins, that some signaling events may differ in their pharmacological profiles and that formation of heterodimers of these receptors may provide new avenues for both signaling and drug design.

摘要

G蛋白偶联受体是主要的药物靶点类别之一,因此了解通过这些受体进行信号传导的机制非常重要。本综述涵盖了G蛋白偶联受体信号传导方面的一些最新进展。已报道了β2肾上腺素能受体的高分辨率结构,以及参与受体激活的几个分子开关。人们还认识到,受体激活后,受体与G蛋白及其亚基可能并不总是分离的。随着人们认识到一些信号传导可能独立于G蛋白发生、一些信号传导事件的药理学特征可能不同以及这些受体异二聚体的形成可能为信号传导和药物设计提供新途径,这些受体信号传导能力的定义已得到相当大的扩展。

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