首页 | 本学科首页   官方微博 | 高级检索  
     


Methylation of the guanidino group of arginine residues prevents citrullination by peptidylarginine deiminase IV
Authors:Hidaka Yuji  Hagiwara Teruki  Yamada Michiyuki
Affiliation:Department of Life Science, School of Science and Engineering, Kinki University, 3-4-1 Kowakae, Higashi-Osaka, Osaka 577-8502, Japan. yuji@life.kindai.ac.jp
Abstract:Peptidylarginine deiminase IV (PAD IV) catalyzes the citrullination of Arg residues of proteins, such as histones. 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.
Keywords:TFA, trifluoroacetic acid   RP-HPLC, reversed phase high performance liquid chromatography   Tris/HCl, tris(hydroxymethyl)aminomethane hydrochloride   DMF, dimethyl formamide   AcOEt, ethyl acetate   MALDI-TOFMS, matrix-assisted laser desorption/ionization time of flight mass spectrometry   DTT, dithiothreitol   ADMA, NG,NG-dimethyl-  smallcaps"  >l-arginine (asymmetric form)   SDMA, NG,NG-dimethyl-  smallcaps"  >l-arginine(symmetric form)
本文献已被 ScienceDirect PubMed 等数据库收录!
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号