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[激素受体与G蛋白偶联相互作用的分子机制]

[The molecular mechanisms of the interaction of hormonal receptors coupled with G-proteins].

作者信息

Voeĭkov V L, Kiselev O G

出版信息

Fiziol Zh SSSR Im I M Sechenova. 1990 Sep;76(9):1138-44.

PMID:1963854
Abstract

In recent years, quite a few structures of the genes coding membrane-bound hormonal receptors, have been revealed, and the recombinant receptors were cloned in heterogeneous systems. The role of the specific sites of a receptor molecule in the latter's functions is reviewed on example of the beta-adrenergic receptor. These functions involve ligand recognition, signal transmission to the GTP-binding protein, and desensitisation of the receptor. Different procedures of the receptor purification are compared. The data on beta-adrenergic modification by serine protease inhibitors and the homology between beta-receptor and chymotrypsin obtained by the authors, are discussed.

摘要

近年来,编码膜结合激素受体的基因的不少结构已被揭示,并且重组受体在异源系统中被克隆出来。以β-肾上腺素能受体为例,对受体分子特定部位在其功能中的作用进行了综述。这些功能包括配体识别、向GTP结合蛋白的信号传递以及受体的脱敏。比较了受体纯化的不同方法。讨论了作者获得的丝氨酸蛋白酶抑制剂对β-肾上腺素能的修饰数据以及β-受体与胰凝乳蛋白酶之间的同源性。

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