Small heat-shock proteins and their potential role in human disease

被引:208
作者
Clark, JI [1 ]
Muchowski, PJ
机构
[1] Univ Washington, Seattle, WA 98195 USA
[2] Max Planck Inst Biochem, Abt Zellulare Biochem, D-82152 Martinsried, Germany
关键词
D O I
10.1016/S0959-440X(99)00048-2
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 elevated expression of stress proteins is considered to be a universal response to adverse conditions, representing a potential mechanism of cellular defense against disease and a potential target for novel therapeutics, including gene therapy and chaperone-modulating reagents. Recently, a single mutation in the small heat-shock protein human alpha B-crystallin was linked to desmin-related myopathy, which is characterized by abnormal intracellular aggregates of intermediate filaments in human muscle. New findings demonstrate that the high level of expression of stress proteins can contribute to an autoimmune response and can protect proteins that contribute to disease processes.
引用
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页码:52 / 59
页数:8
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共 83 条
[11]  
2-M
[12]   Probing the structure and interactions of crystallin proteins by NMR spectroscopy [J].
Carver, JA .
PROGRESS IN RETINAL AND EYE RESEARCH, 1999, 18 (04) :431-462
[13]   Influence of protein-glutathione mixed disulfide on the chaperone-like function of alpha-crystallin [J].
Cherian, M ;
Smith, JB ;
Jiang, XY ;
Abraham, EC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (46) :29099-29103
[14]   Intrapolypeptide disulfides in human αA-crystallin and their effect on chaperone-like function [J].
Cherian-Shaw M. ;
Smith J.B. ;
Jiang X.-Y. ;
Abraham E.C. .
Molecular and Cellular Biochemistry, 1999, 199 (1-2) :163-167
[15]  
CHYLACK LT, 1999, CRC MOD NUT, P25
[16]   Modulation of the chaperon-like activity of bovine alpha-crystallin [J].
Clark, JI ;
Huang, QL .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (26) :15185-15189
[17]  
CLARK JI, 1999, CRC MOD NUT, P117
[18]  
Cotto JJ, 1999, BIOCHEM SOC SYMP, P105
[19]   Differential temperature-dependent chaperone-like activity of αA- and αB-crystallin homoaggregates [J].
Datta, SA ;
Rao, CM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (49) :34773-34778
[20]   The cardiomyopathy and lens cataract mutation in αB-crystallin alters its protein structure, chaperone activity, and interaction with intermediate filaments in vitro [J].
Der Perng, M ;
Muchowski, PJ ;
van den IJssel, P ;
Wu, GJS ;
Hutcheson, AM ;
Clark, JI ;
Quinlan, RA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (47) :33235-33243