Kinetics of 3-nitrotyrosine modification on exposure to hypochlorous acid

被引:5
作者
Curtis, M. P. [1 ]
Neidigh, J. W. [1 ]
机构
[1] Loma Linda Univ, Sch Med, Dept Basic Sci, Loma Linda, CA 92350 USA
关键词
3-chlorotyrosine; chloramine; biomarker; reactive species; protein damage; APOLIPOPROTEIN-A-I; MEDIATED PROTEIN OXIDATION; NITRIC-OXIDE SYNTHASE; HUMAN NEUTROPHILS; TYROSYL RESIDUES; NITRATION; MYELOPEROXIDASE; CHLORINATION; 3-CHLOROTYROSINE; PEROXYNITRITE;
D O I
10.3109/10715762.2014.954110
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
The markers 3-nitrotyrosine and 3-chlorotyrosine are measured as surrogates for reactive nitrogen species and hypochlorous acid respectively, which are both elevated in inflamed human tissues. Previous studies reported a loss of 3-nitrotyrosine when exposed to hypochlorous acid, suggesting that observations of 3-nitrotyrosine underestimate the presence of reactive nitrogen species in diseased tissue (Whiteman and Halliwell, Biochemical and Biophysical Research Communications, 258, 168-172 (1999)). This report evaluates the significance of 3-nitrotyrosine loss by measuring the kinetics of the reaction between 3-nitrotyrosine and hypochlorous acid. The results demonstrate that 3-nitrotyrosine is chlorinated by hypochlorous acid or chloramines to form 3-chloro-5-nitrotyrosine. As 3-nitrotyrosine from in vivo samples is usually found within proteins rather than as free amino acid, we also examined the reaction of 3-nitrotyrosine modification in the context of peptides. The chlorination of 3-nitrotyrosine in peptides was observed to occur up to 700-fold faster than control reactions using equivalent amino acid mixtures. These results further advance our understanding of tyrosine chlorination and the use of 3-nitrotyrosine formed in vivo as a biomarker of reactive nitrogen species.
引用
收藏
页码:1355 / 1362
页数:8
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