Seeing Citrulline: Development of a Phenylglyoxal-Based Probe To Visualize Protein Citrullination

被引:100
作者
Bicker, Kevin L. [1 ]
Subramanian, Venkataraman [1 ]
Chumanevich, Alexander A. [2 ]
Hofseth, Lorne J. [2 ]
Thompson, Paul R. [1 ]
机构
[1] Scripps Florida, Scripps Res Inst, Dept Chem, Jupiter, FL 33458 USA
[2] Univ S Carolina, S Carolina Coll Pharm, Dept Pharmaceut & Biomed Sci, Columbia, SC 29201 USA
关键词
PEPTIDYLARGININE DEIMINASE; RHEUMATOID-ARTHRITIS; ARGININE DEIMINASE-4; PAD4; COLITIS; INACTIVATORS; EXPRESSION; INHIBITORS;
D O I
10.1021/ja308871v
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
Protein arginine deiminases (PADs) catalyze the hydrolysis of peptidyl arginine to form peptidyl citrulline. Abnormally high PAD activity is observed in a host of human diseases, but the exact role of protein citrullination in these diseases and the identities of specific citrullinated disease biomarkers remain unknown, largely because of the lack of readily available chemical probes to detect protein citrullination. For this reason, we developed a citrulline-specific chemical probe, rhodamine-phenylglyoxal (Rh PG), which we show can be used to investigate protein citrullination. This methodology is superior to existing techniques because it possesses higher throughput and excellent sensitivity. Additionally, we demonstrate that this probe can be used to determine the kinetic parameters for a number of protein substrates, monitor drug efficacy, and identify disease biomarkers in an animal model of ulcerative colitis that displays aberrantly increased PAD activity.
引用
收藏
页码:17015 / 17018
页数:4
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