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激动剂和拮抗剂在G蛋白偶联受体上的非排他性结合模型。

A model of non-exclusive binding of agonist and antagonist on G-protein coupled receptors.

作者信息

Järv J

机构信息

Institute of Chemical Physics, University of Tartu, Estonia.

出版信息

J Theor Biol. 1995 Aug 21;175(4):577-82. doi: 10.1006/jtbi.1995.0166.

Abstract

A modified concept of functioning of G-protein coupled receptors is presented, on the assumption that agonistic and antagonistic effects of drugs are related to their interaction with two separate receptor sites that exist simultaneously on a single receptor molecule and possess different ligand-specificity patterns. This proposal distinguishes between agonists and antagonists as binding at one of these sites triggers the receptor response, whereas the other site elicits another response leading to the receptor blockade. As these sites are simultaneously present on a single receptor molecule the formation of a ternary complex between agonist, antagonist and receptor is possible. Practical consequences of this concept are analysed with reference to experimental data on muscarinic acetylcholine receptors.

摘要

本文提出了一种G蛋白偶联受体功能的修正概念,假设药物的激动和拮抗作用与其与单个受体分子上同时存在的两个独立受体位点的相互作用有关,这两个位点具有不同的配体特异性模式。该提议区分了激动剂和拮抗剂,因为在这些位点之一上的结合会触发受体反应,而另一个位点会引发另一种导致受体阻断的反应。由于这些位点同时存在于单个受体分子上,激动剂、拮抗剂和受体之间形成三元复合物是可能的。参照毒蕈碱型乙酰胆碱受体的实验数据分析了这一概念的实际影响。

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