The 26 S Proteasome: From Basic Mechanisms to Drug Targeting

被引:144
|
作者
Navon, Ami [1 ]
Ciechanover, Aaron [2 ,3 ]
机构
[1] Weizmann Inst Sci, Dept Regulat Biol, IL-76100 Rehovot, Israel
[2] Technion Israel Inst Technol, Canc & Vasc Biol Res Ctr, Rappaport Fac Med, IL-31096 Haifa, Israel
[3] Technion Israel Inst Technol, Res Inst, IL-31096 Haifa, Israel
基金
以色列科学基金会;
关键词
NF-KAPPA-B; UNFOLDED PROTEIN RESPONSE; 20S PROTEASOME; MULTIUBIQUITIN-CHAIN; MULTIPLE-MYELOMA; UBIQUITIN CHAINS; CRYSTAL-STRUCTURE; ANTICANCER DRUGS; CANCER-THERAPY; CORE PARTICLE;
D O I
10.1074/jbc.R109.018481
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 regulated degradation of proteins within eukaryotes and bacterial cells is catalyzed primarily by large multimeric proteases in ATP-dependent manner. In eukaryotes, the 26 S proteasome is essential for the rapid destruction of key regulatory proteins, such as cell cycle regulators and transcription factors, whose fast and tuned elimination is necessary for the proper control of the fundamental cell processes they regulate. In addition, the 26 S proteasome is responsible for cell quality control by eliminating defective proteins from the cytosol and endoplasmic reticulum. These defective proteins can be misfolded proteins, nascent prematurely terminated polypeptides, or proteins that fail to assemble into complexes. These diverse activities and its central role in apoptosis have made the proteasome an important target for drug development, in particular to combat malignancies.
引用
收藏
页码:33713 / 33718
页数:6
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