Division of Medicinal Chemistry, Leiden/Amsterdam Centre for Drug Research, Leiden University, P.O. Box 9502, 2300 RA Leiden, The Netherlands.
Trends Pharmacol Sci. 2011 Jan;32(1):35-42. doi: 10.1016/j.tips.2010.10.001.
G protein-coupled receptors (GPCRs) are the major drug target of medicines on the market today. Therefore, much research is and has been devoted to the elucidation of the function and three-dimensional structure of this large family of membrane proteins, which includes multiple conserved transmembrane domains connected by intra- and extracellular loops. In the last few years, the less conserved extracellular loops have garnered increasing interest, particularly after the publication of several GPCR crystal structures that clearly show the extracellular loops to be involved in ligand binding. This review will summarize the recent progress made in the clarification of the ligand binding and activation mechanism of class-A GPCRs and the role of extracellular loops in this process.
G 蛋白偶联受体(GPCRs)是当今市场上药物的主要药物靶点。因此,人们投入了大量的研究来阐明这个由多个跨膜结构域组成的大型膜蛋白家族的功能和三维结构,这些结构域由细胞内和细胞外环连接。在过去的几年中,人们对不太保守的细胞外环越来越感兴趣,特别是在发表了几个 GPCR 晶体结构之后,这些结构清楚地表明细胞外环参与了配体结合。这篇综述将总结最近在阐明 A 类 GPCR 配体结合和激活机制以及细胞外环在这一过程中的作用方面取得的进展。