Citrullination:: A posttranslational modification in health and disease

被引:372
作者
Gyorgy, Bence
Toth, Erzsbet
Tarcsa, Edit
Falus, Andras
Buzas, Edit I.
机构
[1] Semmelweis Univ, Dept Genet Cell & Immunobiol, H-1089 Budapest, Hungary
[2] Semmelweis Univ, Dept Med Biochem, H-1085 Budapest, Hungary
[3] Abbott Biores Ctr, Worcester, MA USA
关键词
biochemistry; autoimmunity; clinical; cell biology; apoptosis;
D O I
10.1016/j.biocel.2006.03.008
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
Posttranslational modifications are chemical changes to proteins that take place after synthesis. One such modification, peptidylarginine to peptidylcitrulline conversion, catalysed by peptidylarginine deiminases, has recently received significant interest in biomedicine. Introduction of citrulline dramatically changes the structure and function of proteins. It has been implicated in several physiological and pathological processes. Physiological processes include epithelial terminal differentiation, gene expression regulation, and apoptosis. Rheumatoid arthritis, multiple sclerosis, and Alzheimer's disease are examples of human diseases where protein citrullination involvement has been demonstrated. In this review, we discuss our current understanding on the importance of protein deimination in these processes. We describe the enzymes catalyzing the reaction, as well as their known protein substrates. We review the citrullinated peptide epitopes that are proposed as disease markers, specifically recognized in certain human autoimmune disorders. The potential autopathogenic role of citrullinated epitopes is also discussed. (c) 2006 Elsevier Ltd. All rights reserved.
引用
收藏
页码:1662 / 1677
页数:16
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