Institute of Pharmacology and Toxicology, University of Würzburg, 97078 Würzburg, Germany; Rudolf Virchow Center, DFG-Research Center for Experimental Biomedicine, University of Würzburg, 97078 Würzburg, Germany.
Institute of Pharmacology and Toxicology, University of Würzburg, 97078 Würzburg, Germany; Rudolf Virchow Center, DFG-Research Center for Experimental Biomedicine, University of Würzburg, 97078 Würzburg, Germany.
Curr Opin Cell Biol. 2014 Apr;27:87-93. doi: 10.1016/j.ceb.2013.11.009. Epub 2013 Dec 17.
The activation of a G protein-coupled receptor is generally triggered by binding of an agonist to the receptor's binding pocket, or, in the case of rhodopsin, by light-induced changes of the pre-bound retinal. This is followed by a series of a conformational changes towards an active receptor conformation, which is capable of signalling to G proteins and other downstream proteins. In the past few years, a number of new techniques have been employed to analyze the kinetics of this activation process, including X-ray crystallographic three-dimensional structures of receptors in the inactive and the active states, NMR studies of labelled receptors, molecular simulations, and optical analyses with fluorescence resonance energy transfer (FRET). Here we review our current understanding of the activation process of GPCRs as well as open questions in the sequence of events ranging from (sub-)microsecond activation by light or agonist binding to millisecond activation of receptors by soluble ligands and the subsequent generation of an intracellular signal.
G 蛋白偶联受体的激活通常是由激动剂与受体结合口袋的结合触发的,或者在视紫红质的情况下,由预先结合的视网膜光诱导的变化触发。这之后是一系列构象变化朝向活性受体构象,该构象能够向 G 蛋白和其他下游蛋白发出信号。在过去的几年中,已经采用了许多新技术来分析这种激活过程的动力学,包括无活性和有活性状态下受体的 X 射线晶体三维结构、标记受体的 NMR 研究、分子模拟以及荧光共振能量转移(FRET)的光学分析。在这里,我们回顾了我们目前对 GPCR 激活过程的理解,以及从(亚)微秒的光或激动剂结合激活到毫秒的可溶性配体激活受体以及随后产生细胞内信号的一系列事件中存在的问题。