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早老素蛋白和信号肽肽酶的结构生物学。

Structural biology of presenilins and signal peptide peptidases.

机构信息

Department of Neuropathology and Neuroscience, Graduate School of Pharmaceutical Sciences, The University of Tokyo, Tokyo 113-0033, Japan.

出版信息

J Biol Chem. 2013 May 24;288(21):14673-80. doi: 10.1074/jbc.R113.463281. Epub 2013 Apr 12.

Abstract

Presenilin and signal peptide peptidase are multispanning intramembrane-cleaving proteases with a conserved catalytic GxGD motif. Presenilin comprises the catalytic subunit of γ-secretase, a protease responsible for the generation of amyloid-β peptides causative of Alzheimer disease. Signal peptide peptidase proteins are implicated in the regulation of the immune system. Both protease family proteins have been recognized as druggable targets for several human diseases, but their detailed structure still remains unknown. Recently, the x-ray structures of some archaeal GxGD proteases have been determined. We review the recent progress in biochemical and biophysical probing of the structure of these atypical proteases.

摘要

早老素和信号肽肽酶是具有保守催化 GxGD 基序的多跨膜内切蛋白酶。早老素包含γ-分泌酶的催化亚基,γ-分泌酶负责生成阿尔茨海默病致病的淀粉样β肽。信号肽肽酶蛋白与免疫系统的调节有关。这两种蛋白酶家族蛋白已被认为是几种人类疾病的可成药靶点,但它们的详细结构仍不清楚。最近,一些古细菌 GxGD 蛋白酶的 X 射线结构已经被确定。我们回顾了这些非典型蛋白酶结构的生化和生物物理探测的最新进展。

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