Methylation of the guanidino group of arginine residues prevents citrullination by peptidylarginine deiminase IV

被引:41
作者
Hidaka, Y
Hagiwara, T
Yamada, M
机构
[1] Kinki Univ, Sch Sci & Engn, Dept Life Sci, Higashiosaka, Osaka 5778502, Japan
[2] Yokohama City Univ, Grad Sch Integrated Sci, Kanazawa Ku, Yokohama, Kanagawa 2360027, Japan
来源
FEBS LETTERS | 2005年 / 579卷 / 19期
关键词
peptidylarginine deiminase; histone; citrullination; methylation; inhibitor;
D O I
10.1016/j.febslet.2005.06.035
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
Peptidylarginine deiminase TV (PAD IV) catalyzes the citrullination of Arg residues of proteins, such as histories. Suzuki et al. recently reported that haplotypes of the PAD IV gene are associated with susceptibility to rheumatoid arthritis. To investigate the mechanism of substrate specificity and inhibitors of PAD IV, a series of the Arg derivatives were synthesized and their reactivity to PAD IV examined. The results suggest that both imino and carboxyl groups are important in the molecular recognition of PAD IV and that methylation of the guanidino group prevents citrullination. In addition, the findings herein show that Bz-N-G-monomethyl-Arg and Bz-N-G,N-G-dimethyl-Arg specifically inhibit citrullination. (c) 2005 Published by Elsevier B.V. on behalf of the Federation of European Biochemical Societies.
引用
收藏
页码:4088 / 4092
页数:5
相关论文
共 23 条
[1]   Structural basis for Ca2+-induced activation of human PAD4 [J].
Arita, K ;
Hashimoto, H ;
Shimizu, T ;
Nakashima, K ;
Yamada, M ;
Sato, M .
NATURE STRUCTURAL & MOLECULAR BIOLOGY, 2004, 11 (08) :777-783
[2]  
Asaga H, 2001, J LEUKOCYTE BIOL, V70, P46
[3]   Comparative analysis of the mouse and human peptidylarginine deiminase gene clusters reveals highly conserved non-coding segments and a new human gene, PADI6 [J].
Chavanas, S ;
Méchin, MC ;
Takahara, H ;
Kawada, A ;
Nachat, R ;
Serre, G ;
Simon, M .
GENE, 2004, 330 :19-27
[4]   A highly sensitive high-performance liquid chromatography-fluorometric method for the assay of peptidylarginine deiminase activity [J].
Chikuma, T ;
Yamada, M ;
Tsuda, A ;
Yamamoto, M ;
Nakashima, K ;
Yajima, R ;
Kato, T .
ANALYTICAL BIOCHEMISTRY, 2000, 285 (02) :230-234
[5]   Histone deimination antagonizes arginine methylation [J].
Cuthbert, GL ;
Daujat, S ;
Snowden, AW ;
Erdjument-Bromage, H ;
Hagiwara, T ;
Yamada, M ;
Schneider, R ;
Gregory, PD ;
Tempst, P ;
Bannister, AJ ;
Kouzarides, T .
CELL, 2004, 118 (05) :545-553
[6]   PROPERTIES OF PEPTIDYLARGININE DEIMINASE FROM THE EPIDERMIS OF NEWBORN RATS [J].
FUJISAKI, M ;
SUGAWARA, K .
JOURNAL OF BIOCHEMISTRY, 1981, 89 (01) :257-263
[7]   cDNA cloning, gene organization and expression analysis of human peptidylarginine deiminase type I [J].
Guerrin, M ;
Ishigami, A ;
Méchin, MC ;
Nachat, R ;
Valmary, S ;
Sebbag, M ;
Simon, M ;
Senshu, T ;
Serre, G .
BIOCHEMICAL JOURNAL, 2003, 370 :167-174
[8]   Deimination of histone H2A and H4 at arginine 3 in HL-60 granulocytes [J].
Hagiwara, T ;
Hidaka, Y ;
Yamada, M .
BIOCHEMISTRY, 2005, 44 (15) :5827-5834
[9]   Deimination of arginine residues in nucleophosmin/B23 and histones in HL-60 granulocytes [J].
Hagiwara, T ;
Nakashima, K ;
Hirano, H ;
Senshu, T ;
Yamada, M .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 290 (03) :979-983
[10]   The micro domain responsible for ligand-binding of guanylyl cyclase C [J].
Hidaka, Y ;
Matsumoto, Y ;
Shimonishi, Y .
FEBS LETTERS, 2002, 526 (1-3) :58-62