Protein misfolding, aggregation, and degradation in disease

被引:60
作者
Gregersen, N
Bolund, L
Bross, P
机构
[1] Aarhus Univ Hosp SKS, Inst Clin Med, Res Unit Mol Med, DK-8200 Aarhus, Denmark
[2] Aarhus Univ Hosp SKS, Dept Human Genet, DK-8200 Aarhus, Denmark
关键词
conformational disease; protein folding; protein quality control; protein misfolding; protein aggregation; protein aggregation diseases;
D O I
10.1385/MB:31:2:141
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
Pathologies associated with protein misfolding have been observed in neurodegenerative diseases such as Alzheimer's disease, metabolic diseases like phenylketonuria, and diseases affecting structural proteins like collagen or keratin. Misfolding of mutant proteins in these and many other diseases may result in premature degradation, formation of toxic aggregates, or incorporation of toxic conformations into structures. We review common traits of these diverse diseases under the unifying view of protein misfolding. The molecular pathogenesis is discussed in the context of protein quality control systems consisting of molecular chaperones and intracellular proteases that assist the folding and supervise the maintenance of the folded structure. Furthermore, genetic and environmental factors that may modify the severity of these diseases are underscored.
引用
收藏
页码:141 / 150
页数:10
相关论文
共 70 条
[1]
[Anonymous], 1993, Human gene mutation
[2]
Loss of m-AAA protease in mitochondria causes complex I deficiency and increased sensitivity to oxidative stress in hereditary spastic paraplegia [J].
Atorino, L ;
Silvestri, L ;
Koppen, M ;
Cassina, L ;
Ballabio, A ;
Marconi, R ;
Langer, T ;
Casari, G .
JOURNAL OF CELL BIOLOGY, 2003, 163 (04) :777-787
[3]
Roles of molecular chaperones in protein misfolding diseases [J].
Barral, JM ;
Broadley, SA ;
Schaffar, G ;
Hartl, FU .
SEMINARS IN CELL & DEVELOPMENTAL BIOLOGY, 2004, 15 (01) :17-29
[4]
Baum Jean, 1999, Current Opinion in Structural Biology, V9, P122, DOI 10.1016/S0959-440X(99)80016-5
[5]
Energetics in the pathogenesis of neurodegenerative diseases [J].
Beal, MF .
TRENDS IN NEUROSCIENCES, 2000, 23 (07) :298-304
[6]
Impairment of the ubiquitin-proteasome system by protein aggregation [J].
Bence, NF ;
Sampat, RM ;
Kopito, RR .
SCIENCE, 2001, 292 (5521) :1552-1555
[7]
Shocking degeneration [J].
Benndorf, R ;
Welsh, MJ .
NATURE GENETICS, 2004, 36 (06) :547-548
[8]
Bross P, 1999, HUM MUTAT, V14, P186, DOI 10.1002/(SICI)1098-1004(1999)14:3<186::AID-HUMU2>3.0.CO
[9]
2-J
[10]
BROSS P, 2003, PROTEIN MISFOLDING D