Departments of Biological Structure and Biochemistry, Biomolecular Structure Center, University of Washington, Box 357420, Seattle, WA 98195, USA.
Acta Crystallogr D Struct Biol. 2018 Jul 1;74(Pt 7):655-670. doi: 10.1107/S2059798318008136. Epub 2018 Jun 27.
Dimers of G protein-coupled receptors (GPCRs) are believed to be important for signaling with their associated G proteins. Low-resolution electron microscopy has shown rhodopsin dimers in native retinal membranes, and CXCR4 dimers have been found in several different crystal structures. Evidence for dimers of other GPCRs is more indirect. An alternative to computational modeling studies is to search for parallel dimers in the packing environments of the reported crystal structures of GPCRs. Two major structural types of GPCR dimers exist (as predicted by others), but there is considerable structural variation within each cluster. The different structural variants described here might reflect different functional properties and should provide a range of model structures for computational and experimental examination.
G 蛋白偶联受体 (GPCR) 的二聚体被认为对于与其相关的 G 蛋白的信号传递很重要。低分辨率电子显微镜已经在天然视网膜膜中显示出视紫红质二聚体,并且在几种不同的晶体结构中已经发现了 CXCR4 二聚体。其他 GPCR 二聚体的证据更加间接。替代计算建模研究的方法是在报道的 GPCR 晶体结构的包装环境中搜索平行二聚体。存在两种主要的 GPCR 二聚体结构类型(如其他人所预测的),但每个簇内都有相当大的结构变化。这里描述的不同结构变体可能反映了不同的功能特性,并应为计算和实验检查提供一系列模型结构。