Institut de Génomique Fonctionnelle, UMR 5203 CNRS - U 661 INSERM - Univ. Montpellier I & II, 141, rue de la cardonille, 34094 Montpellier Cedex 05, France.
Curr Opin Struct Biol. 2012 Aug;22(4):482-90. doi: 10.1016/j.sbi.2012.03.007. Epub 2012 Apr 3.
G protein-coupled receptors (GPCRs) play a major role in intercellular communication by binding small diffusible ligands (agonists) at the extracellular surface. Agonist-binding induces a conformational change in the receptor, which results in the binding and activation of heterotrimeric G proteins within the cell. Ten agonist-bound structures of non-rhodopsin GPCRs published last year defined for the first time the molecular details of receptor activated states and how inverse agonists, partial agonists and full agonists bind to produce different effects on the receptor. In addition, the structure of the β(2)-adrenoceptor coupled to a heterotrimeric G protein showed how the opening of a cleft in the cytoplasmic face of the receptor as a consequence of agonist binding results in G protein coupling and activation of the G protein.
G 蛋白偶联受体 (GPCRs) 通过在细胞外表面结合小的可扩散配体 (激动剂) 在细胞间通讯中发挥主要作用。激动剂结合诱导受体构象变化,导致细胞内异三聚体 G 蛋白的结合和激活。去年发表的十个非视紫红质 GPCR 的激动剂结合结构首次定义了受体激活状态的分子细节,以及反向激动剂、部分激动剂和完全激动剂如何结合产生对受体的不同影响。此外,与异三聚体 G 蛋白偶联的β(2)-肾上腺素受体的结构表明,受体胞质面裂的打开如何导致 G 蛋白结合和 G 蛋白的激活,这是由于激动剂结合的结果。