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γ-分泌酶复合物:膜内蛋白水解机制

The gamma-secretase complex: machinery for intramembrane proteolysis.

作者信息

Iwatsubo Takeshi

机构信息

Department of Neuropathology and Neuroscience, Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo Bunkyoku, Tokyo 113-0033, Japan.

出版信息

Curr Opin Neurobiol. 2004 Jun;14(3):379-83. doi: 10.1016/j.conb.2004.05.010.

Abstract

Gamma-secretase is a membrane protease complex that possesses presenilin as a catalytic subunit. Presenilin generates amyloid beta peptides in the brains of Alzheimer's patients and is indispensable to Notch signaling in tissue development and renewal. Recent studies have revealed how presenilin is assembled with its cofactor proteins and acquires the gamma-secretase activity: Aph-1 and nicastrin initially form a subcomplex to bind and stabilize presenilin, and then Pen-2 confers the gamma-secretase activity and facilitates endoproteolysis of presenilin. Understanding the mechanism of gamma-secretase cleavage will help to clarify how intercellular cell signaling through transmembrane proteins is regulated by intramembrane proteolysis, and will hopefully eventually lead to a cure for Alzheimer's disease.

摘要

γ-分泌酶是一种膜蛋白酶复合体,它以早老素作为催化亚基。早老素在阿尔茨海默病患者的大脑中产生β淀粉样肽,并且在组织发育和更新过程中的Notch信号传导中不可或缺。最近的研究揭示了早老素如何与其辅助因子蛋白组装并获得γ-分泌酶活性:Aph-1和尼卡斯特林最初形成一个亚复合体以结合并稳定早老素,然后Pen-2赋予γ-分泌酶活性并促进早老素的内蛋白水解。了解γ-分泌酶切割的机制将有助于阐明跨膜蛋白介导的细胞间信号传导是如何通过膜内蛋白水解来调节的,并且有望最终找到治愈阿尔茨海默病的方法。

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