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胞质芳香族氨基酸在毒蕈碱受体介导的磷脂酶C激活中的功能作用

Functional role of a cytoplasmic aromatic amino acid in muscarinic receptor-mediated activation of phospholipase C.

作者信息

Blüml K, Mutschler E, Wess J

机构信息

Laboratory of Bioorganic Chemistry, NIDDKD, National Institutes of Health, Bethesda, Maryland 20892.

出版信息

J Biol Chem. 1994 Apr 15;269(15):11537-41.

PMID:8157684
Abstract

The N-terminal portion of the third intracellular loop (i3) of muscarinic acetylcholine and other G protein-coupled receptors has been shown to largely determine the G protein coupling profile of a given receptor subtype. Using the rat m3 muscarinic receptor as a model system, we have recently demonstrated that a tyrosine residue (Tyr-254), located at the beginning of the i3 domain, is critically involved in muscarinic receptor-mediated stimulation of phosphatidylinositol (PI) hydrolysis (Blüml, K., Mutschler, E., and Wess, J. (1994) J. Biol. Chem. 269, 402-405). This study was designed to investigate the functional role of this amino acid in further molecular detail. Replacement of Tyr-254 (rat m3 receptor) with alanine or exchange of its position with Ile-253 virtually abolished receptor-mediated stimulation of PI hydrolysis studied in transfected COS-7 cells. In contrast, substitution of Tyr-254 by other aromatic residues such as phenylalanine or tryptophan resulted in mutant receptors that behaved functionally similar to the wild type m3 receptor. Introduction of Tyr-254 into the corresponding position (Ser-210) of the m2 muscarinic receptor (which is only poorly coupled to PI turnover) did not result in an enhanced PI response. However, "reinsertion" of Tyr-254 into a functionally inactive chimeric m3/m2 muscarinic receptor (containing m2 receptor sequence at the N terminus of the i3 loop) yielded a mutant receptor that was able to stimulate PI hydrolysis to a similar maximum extent as the wild type m3 receptor. Taken together, our data provide strong evidence that muscarinic receptor-mediated stimulation of PI metabolism is critically dependent on the presence and proper positioning of an aromatic residue at the beginning of the i3 loop.

摘要

毒蕈碱型乙酰胆碱受体及其他G蛋白偶联受体的第三个细胞内环(i3)的N端部分,已被证明在很大程度上决定了特定受体亚型的G蛋白偶联特征。以大鼠m3毒蕈碱型受体作为模型系统,我们最近证实,位于i3结构域起始处的一个酪氨酸残基(Tyr-254),在毒蕈碱型受体介导的磷脂酰肌醇(PI)水解刺激中起关键作用(布卢姆尔,K.,穆施勒,E.,和韦斯,J.(1994年)《生物化学杂志》269,402 - 405)。本研究旨在更深入地从分子层面研究该氨基酸的功能作用。用丙氨酸取代Tyr-254(大鼠m3受体)或将其位置与Ile-253交换,几乎完全消除了在转染的COS-7细胞中研究的受体介导的PI水解刺激。相反,用其他芳香族残基如苯丙氨酸或色氨酸取代Tyr-254,产生的突变受体在功能上与野生型m3受体相似。将Tyr-254引入m2毒蕈碱型受体的相应位置(Ser-210,该受体与PI周转的偶联较差)并未导致PI反应增强。然而,将Tyr-254“重新插入”到功能失活的嵌合m3/m2毒蕈碱型受体(在i3环的N端含有m2受体序列)中,产生了一种突变受体,其能够刺激PI水解,最大程度与野生型m3受体相似。综上所述,我们的数据提供了强有力的证据,表明毒蕈碱型受体介导的PI代谢刺激关键取决于i3环起始处芳香族残基的存在和正确定位。

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