Nicoli Alessandro, Dunkel Andreas, Giorgino Toni, de Graaf Chris, Di Pizio Antonella
Leibniz Institute for Food Systems Biology at the Technical University of Munich, 85354 Freising, Germany.
Biophysics Institute, National Research Council (CNR-IBF), 20133 Milan, Italy.
J Chem Inf Model. 2022 Feb 14;62(3):511-522. doi: 10.1021/acs.jcim.1c01056. Epub 2022 Feb 3.
The extracellular loop 2 (ECL2) is the longest and the most diverse loop among class A G protein-coupled receptors (GPCRs). It connects the transmembrane (TM) helices 4 and 5 and contains a highly conserved cysteine through which it is bridged with TM3. In this paper, experimental ECL2 structures were analyzed based on their sequences, shapes, and intramolecular contacts. To take into account the flexibility, we incorporated into our analyses information from the molecular dynamics trajectories available on the GPCRmd website. Despite the high sequence variability, shapes of the analyzed structures, defined by the backbone volume overlaps, can be clustered into seven main groups. Conformational differences within the clusters can be then identified by intramolecular interactions with other GPCR structural domains. Overall, our work provides a reorganization of the structural information of the ECL2 of class A GPCR subfamilies, highlighting differences and similarities on sequence and conformation levels.
细胞外环2(ECL2)是A类G蛋白偶联受体(GPCR)中最长且最多样化的环。它连接跨膜(TM)螺旋4和5,并包含一个高度保守的半胱氨酸,通过该半胱氨酸与TM3桥接。在本文中,基于实验性ECL2结构的序列、形状和分子内接触进行了分析。为了考虑其灵活性,我们在分析中纳入了来自GPCRmd网站上分子动力学轨迹的信息。尽管序列变异性很高,但由主链体积重叠定义的分析结构形状可聚类为七个主要组。然后可以通过与其他GPCR结构域的分子内相互作用来识别簇内的构象差异。总体而言,我们的工作对A类GPCR亚家族ECL2的结构信息进行了重新整理,突出了序列和构象水平上的差异和相似性。