The Logic of the 26S Proteasome

被引:683
作者
Collins, Galen Andrew [1 ]
Goldberg, Alfred L. [1 ]
机构
[1] Harvard Med Sch, Dept Cell Biol, 240 Longwood Ave, Boston, MA 02115 USA
关键词
MOLECULAR-WEIGHT PROTEASES; BRANCHED UBIQUITIN CHAINS; 20 S PROTEASOMES; PROTEIN-DEGRADATION; DEUBIQUITINATING ENZYME; REGULATORY PARTICLE; FUNCTIONAL ASYMMETRIES; EUKARYOTIC PROTEASOME; MEDIATED DEGRADATION; MISFOLDED PROTEINS;
D O I
10.1016/j.cell.2017.04.023
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:792 / 806
页数:15
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