受体偶联到(多个)G蛋白的调控。对基础研究和药物发现的挑战。

Jyrki P Kukkonen
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引用次数: 37

摘要

G蛋白偶联受体通过与胞质/外周膜蛋白(主要是G蛋白)相互作用诱导胞内信号。关于受体、G蛋白和效应物之间的相互作用模式、它们的移动性以及确定相互作用特异性的方法一直存在很多争论。在发现i)单个受体与几种G蛋白的偶联以及ii)不同配体对这种偶联的活性方向(刺激运输)后,系统增加了额外的复杂性。这些数据表明,信号转导中最主要的单位是受体与特定G蛋白的复合物,这使得对受体-G蛋白选择和相互作用机制的研究变得更加重要。本文综述了受体与G蛋白和效应物相互作用的一般知识及其研究方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Regulation of receptor-coupling to (multiple) G proteins. A challenge for basic research and drug discovery.

G protein-coupled receptors induce intracellular signals via interaction of with cytosolic/peripheral membrane proteins, mainly G proteins. There has been much debate about the mode of interaction between the receptors, G proteins and effectors, their mobility and the ways of determining the specificity of interaction. Additional complexity has been added to system upon the discovery of i) coupling of single receptors to several G proteins and ii) active direction of this by different ligands (stimulus trafficking). These data suggest that the most primary unit in the signal transduction is the receptor complexed with a specific G protein, making the investigation of the mechanism of receptor-G protein selection and interaction even more important. In this review, I will summarize the general knowledge of receptor interaction with G proteins and effectors and the ways of investigating this.

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