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硝基酪氨酸的定量蛋白质组图谱分析

Quantitative proteome mapping of nitrotyrosines.

作者信息

Bigelow Diana J, Qian Wei-Jun

机构信息

Cell Biology and Biochemistry Group, Division of Biological Sciences, Pacific Northwest National Laboratory, Richland, Washington, USA.

出版信息

Methods Enzymol. 2008;440:191-205. doi: 10.1016/S0076-6879(07)00811-7.

Abstract

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.

摘要

了解疾病和环境扰动的一个必不可少的第一步是,与组织或细胞蛋白质组中的内源性水平相比,早期定量检测炎症标志物硝基酪氨酸水平的升高。因此,能够成功实现全蛋白质组范围内硝基酪氨酸及相关氧化修饰定量分析的方法,可提供疾病风险和进展的早期生物标志物,以及有效的治疗策略。近年来,多维分离液相色谱与串联质谱联用(LC-MS/MS)极大地拓展了我们对人类(以及哺乳动物模型系统)蛋白质组的认识,包括在翻译后修饰鉴定方面的一些新进展。本章将在哺乳动物蛋白质组中复杂蛋白质混合物的背景下,讨论LC-MS/MS在定量和鉴定硝基酪氨酸修饰蛋白方面的应用。

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