Racemization of aspartic acid in human proteins

被引:146
作者
Ritz-Timme, S
Collins, MJ [1 ]
机构
[1] Newcastle Univ, Fossil Fuels & Environm Geochem NRG, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
[2] Univ Kiel, Inst Rechts Med, D-24105 Kiel, Germany
关键词
aspartic acid; racemization; review; succinimide; deamidation; collagen;
D O I
10.1016/S0047-6374(01)00363-3
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Aspartic acid racemization (AAR) represents one of the major types of non-enzymatic covalent modification that leads to an age-dependent accumulation of abnormal protein in numerous human tissues. In vivo racemization is an autonomic process during the 'natural' ageing of proteins, and correlates with the age of long-lived proteins. Consequently AAR can be used as molecular indicator of protein ageing as well as for the identification of permanent proteins that age with the human organism. Although long-living, structural proteins are mainly affected, AAR may be significant on a time scale also relevant to enzymes and signaling proteins. It may result in a loss of protein function due to proteolysis or due to changes in the molecular structure. In vivo racemization may also increase in pathological conditions. AAR has already been discussed as a relevant pathophysiological factor in the pathogenesis of diseases of old age such as atherosclerosis, lung emphysema, presbyopia, cataract, degenerative diseases of cartilage and cerebral age-related dysfunctions. Although the details of the biological consequences of AAR have to be further elucidated, it is evident that AAR plays a role in the molecular biology of ageing. (C) 2002 Elsevier Science Ireland Ltd. All rights reserved.
引用
收藏
页码:43 / 59
页数:17
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