Quantitative proteome mapping of nitrotyrosines

被引:20
作者
Bigelow, Diana J. [1 ]
Qian, Wei-Jun [2 ]
机构
[1] Pacific NW Natl Lab, Cell Biol & Biochem Grp, Div Biol Sci, Richland, WA 99352 USA
[2] Pacific NW Natl Lab, Environm Mol Sci Lab, Div Biol Sci, Richland, WA 99352 USA
来源
NITRIC OXIDE, PART F: OXIDATIVE AND NITROSATIVE STRESS IN REDOX REGULATION OF CELL SIGNALING | 2008年 / 440卷
关键词
D O I
10.1016/S0076-6879(07)00811-7
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An essential first step in the understanding disease and environmental perturbations is the early and quantitative detection of the increased levels of the inflammatory marker nitrotyrosine, as compared with its endogenous levels within the tissue or cellular proteome. Thus, methods that successfully address a proteome-wide quantitation of nitrotyrosine and related oxidative modifications can provide early biomarkers of risk and progression of disease, as well as effective strategies for therapy. Multidimensional separations LC coupled with tandem mass spectrometry (LC-MS/MS) has, in recent years, significantly expanded our knowledge of human (and mammalian model system) proteomes, including some nascent work in identification of posttranslational modifications. This chapter discusses the application of LC-MS/MS for quantitation and identification of nitrotyrosine-modified proteins within the context of complex protein mixtures presented in mammalian proteomes.
引用
收藏
页码:191 / 205
页数:15
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