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G 蛋白偶联受体的分子特征。

Molecular signatures of G-protein-coupled receptors.

机构信息

MRC Laboratory of Molecular Biology, Hills Road, Cambridge CB2 0QH, UK.

出版信息

Nature. 2013 Feb 14;494(7436):185-94. doi: 10.1038/nature11896.

Abstract

G-protein-coupled receptors (GPCRs) are physiologically important membrane proteins that sense signalling molecules such as hormones and neurotransmitters, and are the targets of several prescribed drugs. Recent exciting developments are providing unprecedented insights into the structure and function of several medically important GPCRs. Here, through a systematic analysis of high-resolution GPCR structures, we uncover a conserved network of non-covalent contacts that defines the GPCR fold. Furthermore, our comparative analysis reveals characteristic features of ligand binding and conformational changes during receptor activation. A holistic understanding that integrates molecular and systems biology of GPCRs holds promise for new therapeutics and personalized medicine.

摘要

G 蛋白偶联受体(GPCRs)是一种在生理上非常重要的膜蛋白,能够感知激素和神经递质等信号分子,也是几种规定药物的靶点。最近令人兴奋的发展为几种医学上重要的 GPCR 的结构和功能提供了前所未有的见解。在这里,我们通过对高分辨率 GPCR 结构的系统分析,揭示了一个保守的非共价相互作用网络,该网络定义了 GPCR 的构象。此外,我们的比较分析揭示了配体结合和受体激活过程中构象变化的特征。对 GPCR 的分子和系统生物学的整体理解有望为新的治疗方法和个性化医疗提供帮助。

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