Activation of G protein-coupled receptors.

Xavier Deupi, Brian Kobilka
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引用次数: 90

Abstract

G protein-coupled receptors (GPCRs) mediate responses to hormones and neurotransmitters, as well as the senses of sight, smell, and taste. These remarkably versatile signaling molecules respond to structurally diverse ligands. Many GPCRs couple to multiple G protein subtypes, and several have been shown to activate G protein-independent signaling pathways. Drugs acting on GPCRs exhibit efficacy profiles that may differ for different signaling cascades. The functional plasticity exhibited by GPCRs can be attributed to structural flexibility and the existence of multiple ligand-specific conformational states. This chapter will review our current understanding of the mechanism by which agonists bind and activate GPCRs.

G蛋白偶联受体的激活。
G蛋白偶联受体(gpcr)介导对激素和神经递质以及视觉、嗅觉和味觉的反应。这些功能多样的信号分子对结构多样的配体做出反应。许多gpcr与多种G蛋白亚型结合,其中一些已被证明可以激活不依赖G蛋白的信号通路。作用于gpcr的药物在不同的信号级联反应中表现出不同的疗效。gpcr所表现出的功能可塑性可归因于结构的灵活性和多种配体特异性构象态的存在。本章将回顾我们目前对激动剂结合和激活gpcr的机制的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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