Ueda H, Nozaki M, Satoh M
Department of Pharmacology, Faculty of Pharmaceutical Sciences, Kyoto University, Japan.
Comp Biochem Physiol C Comp Pharmacol Toxicol. 1991;98(1):157-69.
We believed that GTP-binding protein (G-protein)-coupling receptor always transduces stimulatory signals to G-proteins. From our recent experiments using reconstitution techniques, however, it was revealed that some receptors transduce an inhibitory or no signal to G-proteins in specific tissues, despite some interaction between them. Here we discuss the molecular basis of mechanisms of such diverse modes of functional coupling between different subtypes of opioid receptors and G-proteins.
我们曾认为鸟苷三磷酸(GTP)结合蛋白(G蛋白)偶联受体总是将刺激性信号转导至G蛋白。然而,根据我们最近采用重组技术进行的实验发现,尽管某些受体与G蛋白之间存在相互作用,但在特定组织中,一些受体却会将抑制性信号或无信号转导至G蛋白。在此,我们将探讨阿片受体不同亚型与G蛋白之间这种功能偶联的多种模式机制的分子基础。