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腺苷酸环化酶的双重调节。膜受体的信号转导机制。

Dual regulation of adenylate cyclase. A signal transduction mechanism of membrane receptors.

作者信息

Jakobs K H, Minuth M, Bauer S, Grandt R, Greiner C, Zubin P

出版信息

Basic Res Cardiol. 1986 Jan-Feb;81(1):1-9. doi: 10.1007/BF01907422.

Abstract

The hormone-sensitive adenylate cyclase is a multi-component system embedded in the lipid bilayer of the plasma membrane and serves as a signal transduction system for various membrane receptors. The complete system consists of various receptor molecules, which sensitize the external ligands, the effector enzyme adenylate cyclase, which catalyzes the formation of cyclic AMP from ATP, and two guanine nucleotide-binding regulatory proteins (N or G proteins), which transduce the signals from the receptors to the adenylate cyclase. Depending on the receptor type activated by a ligand, stimulatory or inhibitory, either the stimulatory or the inhibitory N protein is activated and induces stimulation or inhibition of adenylate cyclase with subsequent increase or decrease in cellular cyclic AMP levels. In this paper, the mechanisms of this hormonal signal transduction system and its regulation will briefly reviewed, with some emphasis on the cardiac system.

摘要

激素敏感型腺苷酸环化酶是一种嵌入质膜脂质双层的多组分系统,作为各种膜受体的信号转导系统。完整的系统由各种受体分子组成,这些受体分子能识别外部配体;效应酶腺苷酸环化酶,它催化ATP形成环磷酸腺苷;还有两种鸟嘌呤核苷酸结合调节蛋白(N蛋白或G蛋白),它们将信号从受体转导至腺苷酸环化酶。根据配体激活的受体类型是刺激性还是抑制性的,刺激性或抑制性N蛋白会被激活,并诱导腺苷酸环化酶的刺激或抑制,随后细胞内环磷酸腺苷水平升高或降低。本文将简要综述这种激素信号转导系统的机制及其调节,重点放在心脏系统。

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