Simultaneous determination of 3-nitrotyrosine and tyrosine in plasma proteins of rats and assessment of artifactual tyrosine nitration

被引:28
作者
Delatour, T
Richoz, J
Vouros, P
Turesky, RJ
机构
[1] Nestec Ltd, Nestle Res Ctr, CH-1000 Lausanne 26, Switzerland
[2] Northeastern Univ, Boston, MA 02115 USA
[3] Natl Ctr Toxicol Res, Div Chem, Jefferson, AR 72079 USA
来源
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES | 2002年 / 779卷 / 02期
关键词
nitration; nitrotyrosine; tyrosine; proteins;
D O I
10.1016/S1570-0232(02)00370-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A sensitive and specific isotope dilution liquid chromatography-electrospray tandem mass spectrometry method was developed for the determination of the 3-nitrotyrosine residue levels in rat plasma proteins. The assay is based on the cleavage of proteins with concentrated hydrochloric acid to release both 3-nitrotyrosine and tyrosine. To control the potential artifactual nitration of tyrosine residues during the proteolysis, samples are spiked with C-13(9)-labeled tyrosine and the level of C-13(9)-labeled 3-nitrotyrosine is measured. The clean-up process entails hydrolysate fortification with 2,5,643-3-nitrotyrosine, followed. by solid-phase extraction on octadecylsilyl (to isolate tyrosine) and aminopropylsilyl (to isolate 3-nitrotyrosine) cartridges. Tyrosine and 3-nitrotyrosine fractions are mixed in an appropriate ratio prior to the analysis. The method was applied to animals exposed to ferric nitrilotriacetate to induce oxidative stress. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:189 / 199
页数:11
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