Miyagi Masaru, Rao K C Sekhar
Case Center for Proteomics, School of Medicine, Case Western Reserve University, Cleveland, Ohio 44106, USA.
Mass Spectrom Rev. 2007 Jan-Feb;26(1):121-36. doi: 10.1002/mas.20116.
A number of proteomic techniques have been developed to quantify proteins in biological systems. This review focuses on the quantitative proteomic technique known as "proteolytic 18O-labeling." This technique utilizes a protease and H(2)18O to produce labeled peptides, with subsequent chromatographic and mass spectrometric analysis to identify and quantify (relative) the proteins from which the peptides originated. The technique determines the ratio of individual protein's expression level between two samples relative to each other, and can be used to quantitatively examine protein expression (comparative proteomics) and post-translational modifications, and to study protein-protein interactions. The present review discusses various aspects of the 18O-labeling technique, including: its history, the advantages and disadvantages of the proteolytic 18O-labeling technique compared to other techniques, enzymatic considerations, the problem of variable incorporation of 18O atoms into peptides with a discussion on recent advancements of the technique to overcome it, computational tools to interpret the data, and a review of the biological applications.
已经开发了许多蛋白质组学技术来定量生物系统中的蛋白质。本综述重点关注称为“蛋白水解18O标记”的定量蛋白质组学技术。该技术利用蛋白酶和H₂¹⁸O产生标记的肽段,随后进行色谱和质谱分析,以鉴定和定量(相对)肽段来源的蛋白质。该技术确定两个样品之间单个蛋白质表达水平的相对比例,可用于定量检测蛋白质表达(比较蛋白质组学)和翻译后修饰,并研究蛋白质-蛋白质相互作用。本综述讨论了18O标记技术的各个方面,包括:其历史、与其他技术相比蛋白水解18O标记技术的优缺点、酶学考虑因素、18O原子在肽段中掺入量可变的问题以及克服该问题的技术最新进展、解释数据的计算工具以及生物应用综述。