Blin N, Yun J, Wess J
Laboratory of Bioorganic Chemistry, NIDDK, National Institutes of Health, Bethesda, Maryland 20892, USA.
J Biol Chem. 1995 Jul 28;270(30):17741-8. doi: 10.1074/jbc.270.30.17741.
Each G protein-coupled receptor can interact only with a limited number of the many structurally similar G proteins expressed within a cell. This study was undertaken to identify single amino acids required for selectively coupling the m3 muscarinic acetylcholine receptor to G proteins of the Gq/11 family. To this goal, distinct intracellular segments/amino acids of the m3 receptor were systematically substituted into the structurally closely related m2 muscarinic receptor, which couples to Gi/o proteins, not Gq/11 proteins. The resultant mutant receptors were expressed in COS-7 cells and studied for their ability to induce agonist-dependent stimulation of phosphatidylinositol hydrolysis, a response known to be mediated by G proteins of the Gq/11 class. Using this approach, we were able to identify four amino acids in the second intracellular loop and four amino acids at the C terminus of the third intracellular loop of the m3 muscarinic receptor that are essential for efficient Gq/11 activation. We could demonstrate that these amino acids, together with a short segment at the N terminus of the third intracellular loop, fully account for the G protein coupling preference of the m3 muscarinic receptor. Taken together, our data strongly suggest that only a limited number of amino acids, located on different intracellular regions, are required to determine the functional profile of a given G protein-coupled receptor.
每个G蛋白偶联受体只能与细胞内表达的众多结构相似的G蛋白中的有限数量相互作用。本研究旨在确定将m3毒蕈碱型乙酰胆碱受体选择性偶联至Gq/11家族G蛋白所需的单个氨基酸。为实现这一目标,将m3受体不同的细胞内片段/氨基酸系统地替换到结构密切相关的m2毒蕈碱型受体中,m2受体与Gi/o蛋白偶联,而非Gq/11蛋白。将所得突变受体在COS-7细胞中表达,并研究其诱导激动剂依赖性磷脂酰肌醇水解刺激的能力,这一反应已知由Gq/11类G蛋白介导。使用这种方法,我们能够确定m3毒蕈碱型受体第二个细胞内环中的四个氨基酸以及第三个细胞内环C末端的四个氨基酸,它们对于有效的Gq/11激活至关重要。我们可以证明,这些氨基酸与第三个细胞内环N末端的一个短片段一起,完全解释了m3毒蕈碱型受体的G蛋白偶联偏好。综上所述,我们的数据强烈表明,仅需位于不同细胞内区域的有限数量的氨基酸即可确定给定G蛋白偶联受体的功能特征。