To be, or not to be -: molecular chaperones in protein degradation

被引:138
作者
Arndt, V. [1 ]
Rogon, C. [1 ]
Hoehfeld, J. [1 ]
机构
[1] Univ Bonn, Inst Zellbiol, D-53121 Bonn, Germany
关键词
CHIP; Parkin; Hsp70; Hsp90; ubiquitin; proteasome;
D O I
10.1007/s00018-007-7188-6
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 [生物化学与分子生物学]; 081704 [应用化学];
摘要
To be, or not to be - that is the question not only for Hamlet in Shakespeare's drama but also for a protein associated with molecular chaperones. While long viewed exclusively as cellular folding factors, molecular chaperones recently emerged as active participants in protein degradation. This places chaperones at the center of a life or death decision during protein triage. Here we highlight molecular mechanisms that underlie chaperone action at the folding/degradation interface in mammalian cells. We discuss the importance of chaperone-assisted degradation for the regulation of cellular processes and its emerging role as a target for therapeutic intervention in cancer and amyloid diseases.
引用
收藏
页码:2525 / 2541
页数:17
相关论文
共 160 条
[1]
CHIP protects from the neurotoxicity of expanded and wild-type ataxin-1 and promotes their ubiquitination and degradation [J].
Al-Ramahi, Ismael ;
Lam, Yung C. ;
Chen, Hung-Kai ;
de Gouyon, Beatrice ;
Zhang, Minghang ;
Perez, Alma M. ;
Branco, Joana ;
de Haro, Maria ;
Patterson, Cam ;
Zoghbi, Huda Y. ;
Botas, Juan .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2006, 281 (36) :26714-26724
[2]
Ubiquitylation of BAG-1 suggests a novel regulatory mechanism during the sorting of chaperone substrates to the proteasome [J].
Alberti, S ;
Demand, J ;
Esser, C ;
Emmerich, N ;
Schild, H ;
Höhfeld, J .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (48) :45920-45927
[3]
The cochaperone HspBP1 inhibits the CHIP ubiquitin ligase and stimulates the maturation of the cystic fibrosis transmembrane conductance regulator [J].
Alberti, S ;
Böhse, K ;
Arndt, V ;
Schmitz, A ;
Höhfeld, J .
MOLECULAR BIOLOGY OF THE CELL, 2004, 15 (09) :4003-4010
[4]
Mechanism and function of deubiquitinating enzymes [J].
Amerik, AY ;
Hochstrasser, M .
BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR CELL RESEARCH, 2004, 1695 (1-3) :189-207
[5]
BAG-2 acts as an inhibitor of the chaperone-associated ubiquitin ligase CHIP [J].
Arndt, V ;
Daniel, C ;
Nastainczyk, W ;
Alberti, S ;
Höhfeld, J .
MOLECULAR BIOLOGY OF THE CELL, 2005, 16 (12) :5891-5900
[6]
Ballinger CA, 1999, MOL CELL BIOL, V19, P4535
[7]
Role of the myosin assembly protein UNC-45 as a molecular chaperone for myosin [J].
Barral, JM ;
Hutagalung, AH ;
Brinker, A ;
Hartl, FU ;
Epstein, HF .
SCIENCE, 2002, 295 (5555) :669-671
[8]
Ubiquitin-proteasome degradation of serum- and glucocorticoid-regulated kinase-1 (SGK-1) is mediated by the chaperone-dependent E3 ligase CHIP [J].
Belova, Larissa ;
Sharma, Sanjay ;
Brickley, Deanna R. ;
Nicolarsen, Jeremy R. ;
Patterson, Cam ;
Conzen, Suzanne D. .
BIOCHEMICAL JOURNAL, 2006, 400 (02) :235-244
[9]
Chaperoning brain degeneration [J].
Bonini, NM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 :16407-16411
[10]
Ubiquitination and proteasomal degradation of nucleophosmin-anaplastic lymphoma kinase induced by 17-allylamino-demethoxygeldanamycin: Role of the co-chaperone carboxyl heat shock protein 70-interacting protein [J].
Bonvini, P ;
Dalla Rosa, H ;
Vignes, N ;
Rosolen, A .
CANCER RESEARCH, 2004, 64 (09) :3256-3264