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Importance of the extracellular loops in G protein-coupled receptors for ligand recognition and receptor activation.

机译:G蛋白偶联受体中细胞外环对于配体识别和受体激活的重要性。

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摘要

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.
机译:G蛋白偶联受体(GPCR)是当今市场上主要的药物靶向药物。因此,关于这种大的膜蛋白家族的功能和三维结构的阐明已经进行了大量的研究,其中包括通过细胞内和细胞外环连接的多个保守的跨膜结构域。在最近几年中,保守性较低的细胞外环引起了越来越多的兴趣,尤其是在公开了几种清楚地表明细胞外环参与配体结合的GPCR晶体结构之后。这篇综述将总结在阐明A类GPCR的配体结合和激活机制以及细胞外环在此过程中的作用方面取得的最新进展。

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