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蛋白磷酸化对间隙连接的调控。

Regulation of gap junctions by protein phosphorylation.

作者信息

Sáez J C, Martínez A D, Brañes M C, González H E

机构信息

Departamento de Ciencias Fisiológicas, Pontificia Universidad Católica de Chile, Santiago, Chile.

出版信息

Braz J Med Biol Res. 1998 May;31(5):593-600. doi: 10.1590/s0100-879x1998000500001.

Abstract

Gap junctions are constituted by intercellular channels and provide a pathway for transfer of ions and small molecules between adjacent cells of most tissues. The degree of intercellular coupling mediated by gap junctions depends on the number of gap junction channels and their activity may be a function of the state of phosphorylation of connexins, the structural subunit of gap junction channels. Protein phosphorylation has been proposed to control intercellular gap junctional communication at several steps from gene expression to protein degradation, including translational and post-translational modification of connexins (i.e., phosphorylation of the assembled channel acting as a gating mechanism) and assembly into and removal from the plasma membrane. Several connexins contain sites for phosphorylation for more than one protein kinase. These consensus sites vary between connexins and have been preferentially identified in the C-terminus. Changes in intercellular communication mediated by protein phosphorylation are believed to control various physiological tissue and cell functions as well as to be altered under pathological conditions.

摘要

间隙连接由细胞间通道构成,为大多数组织中相邻细胞之间的离子和小分子转移提供了一条途径。由间隙连接介导的细胞间偶联程度取决于间隙连接通道的数量,其活性可能是连接蛋白(间隙连接通道的结构亚基)磷酸化状态的函数。有人提出,蛋白质磷酸化在从基因表达至蛋白质降解的多个步骤中控制细胞间间隙连接通讯,包括连接蛋白的翻译和翻译后修饰(即组装好的通道的磷酸化作为一种门控机制)以及组装到质膜和从质膜上移除。几种连接蛋白含有不止一种蛋白激酶的磷酸化位点。这些共有位点在不同连接蛋白之间有所不同,并且已在C末端被优先鉴定出来。据信,由蛋白质磷酸化介导的细胞间通讯变化可控制各种生理组织和细胞功能,并且在病理条件下也会发生改变。

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