Department of Chemistry and Pharmacy, Emil Fischer Center, Friedrich Alexander University , Schuhstraße 19, 91052 Erlangen, Germany.
J Med Chem. 2013 Sep 12;56(17):6542-59. doi: 10.1021/jm4004335. Epub 2013 Jun 4.
G-protein-coupled receptors (GPCRs) represent the largest family of membrane proteins involved in cellular signal transduction and are activated by various different ligand types including photons, peptides, proteins, but also small molecules like biogenic amines. Therefore, GPCRs are involved in diverse physiological processes and provide valuable drug targets for numerous diseases. Emerging body of evidence suggests that GPCRs exist as monomers or cross-react forming dimers and higher-ordered oligomers. In this Perspective we will review current biochemical and biophysical techniques to visualize GPCR dimerization, functional consequences of homo- and heterodimers, and approaches of medicinal chemists to target these receptor complexes with homo- and heterobivalent ligands.
G 蛋白偶联受体 (GPCRs) 是参与细胞信号转导的最大膜蛋白家族,可被各种不同的配体类型激活,包括光子、肽、蛋白质,甚至小分子如生物胺。因此,GPCRs 参与多种生理过程,并为许多疾病提供了有价值的药物靶点。越来越多的证据表明,GPCR 以单体形式存在或相互作用形成二聚体和更高阶的寡聚体。在这篇观点文章中,我们将回顾当前用于可视化 GPCR 二聚化的生化和生物物理技术、同型和异型二聚体的功能后果,以及药物化学家使用同型和异型双价配体靶向这些受体复合物的方法。