Hein Peter, Bünemann Moritz
Department of Psychiatry, University of California at San Francisco, 600 16th St, UCSF MC 2140, Genentech Hall N216P, San Francisco, CA 94158-2517, USA.
Naunyn Schmiedebergs Arch Pharmacol. 2009 May;379(5):435-43. doi: 10.1007/s00210-008-0383-7. Epub 2008 Dec 2.
Signaling via G-protein-coupled receptors (GPCRs) is crucial to many physiological and pathophysiological processes in multicellular organisms, and GPCRs themselves are targets for important drugs. Classical cell supplementation experiments suggest a collision coupling model, in which receptors and G proteins diffuse randomly within the cell membrane and interact only if receptors are activated. This model is also backed by kinetic and live cell imaging data. According to the challenging theory, receptors and G proteins are precoupled--meaning they are forming stable complexes in the absence of agonist, which prevail during signaling. This model has been favored on the basis of copurification and coimmunoprecipitation of inactive receptors with G proteins and more recently by some approaches measuring energy transfer between labeled receptors and G proteins. This article reviews key findings regarding the receptor/G protein coupling mode, including most recent findings obtained by optical techniques.
通过G蛋白偶联受体(GPCRs)进行信号传导对多细胞生物中的许多生理和病理生理过程至关重要,并且GPCRs本身就是重要药物的靶点。经典的细胞补充实验提出了一种碰撞偶联模型,即受体和G蛋白在细胞膜内随机扩散,只有受体被激活时才会相互作用。该模型也得到了动力学和活细胞成像数据的支持。根据这一具有挑战性的理论,受体和G蛋白是预偶联的——这意味着它们在没有激动剂的情况下形成稳定的复合物,在信号传导过程中占主导地位。基于无活性受体与G蛋白的共纯化和共免疫沉淀,以及最近一些测量标记受体与G蛋白之间能量转移的方法,该模型受到了青睐。本文综述了关于受体/G蛋白偶联模式的关键发现,包括通过光学技术获得的最新发现。