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26S蛋白酶体的逻辑

The Logic of the 26S Proteasome.

作者信息

Collins Galen Andrew, Goldberg Alfred L

机构信息

Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.

Department of Cell Biology, Harvard Medical School, 240 Longwood Avenue, Boston, MA 02115, USA.

出版信息

Cell. 2017 May 18;169(5):792-806. doi: 10.1016/j.cell.2017.04.023.

Abstract

The ubiquitin proteasome pathway is responsible for most of the protein degradation in mammalian cells. Rates of degradation by this pathway have generally been assumed to be determined by rates of ubiquitylation. However, recent studies indicate that proteasome function is also tightly regulated and determines whether a ubiquitylated protein is destroyed or deubiquitylated and survives longer. This article reviews recent advances in our understanding of the proteasome's multistep ATP-dependent mechanism, its biochemical and structural features that ensure efficient proteolysis and ubiquitin recycling while preventing nonselective proteolysis, and the regulation of proteasome activity by interacting proteins and subunit modifications, especially phosphorylation.

摘要

泛素蛋白酶体途径负责哺乳动物细胞中大部分蛋白质的降解。通常认为该途径的降解速率由泛素化速率决定。然而,最近的研究表明,蛋白酶体功能也受到严格调控,并决定泛素化蛋白质是被降解还是去泛素化并存活更长时间。本文综述了我们对蛋白酶体多步ATP依赖机制、其生化和结构特征(确保有效蛋白水解和泛素循环,同时防止非选择性蛋白水解)以及通过相互作用蛋白和亚基修饰(特别是磷酸化)对蛋白酶体活性的调控的最新认识进展。

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