Isobaric Labeling-Based Relative Quantification in Shotgun Proteomics

被引:420
|
作者
Rauniyar, Navin [1 ]
Yates, John R., III [1 ]
机构
[1] Scripps Res Inst, Dept Physiol Chem, La Jolla, CA 92037 USA
关键词
iTRAQ; isobaric tags for relative and absolute quantification; TMT; tandem mass tags; isobaric tags; isobaric labeling; quantitative proteomics; mass spectrometry; TANDEM MASS TAGS; 2-DIMENSIONAL LIQUID-CHROMATOGRAPHY; COMPLEX PROTEIN MIXTURES; QUANTITATIVE PROTEOMICS; RATIO COMPRESSION; TAGGING REAGENTS; ENABLES ACCURATE; CANCER CELLS; ITRAQ; SPECTROMETRY;
D O I
10.1021/pr500880b
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Mass spectrometry plays a key role in relative quantitative comparisons of proteins in order to understand their functional role in biological systems upon perturbation. In this review, we review studies that examine different aspects of isobaric labeling-based relative quantification for shotgun proteomic analysis. In particular, we focus on different types of isobaric reagents and their reaction chemistry (e.g., amine-, carbonyl-, and sulfhydryl-reactive). Various factors, such as ratio compression, reporter ion dynamic range, and others, cause an underestimation of changes in relative abundance of proteins across samples, undermining the ability of the isobaric labeling approach to be truly quantitative. These factors that affect quantification and the suggested combinations of experimental design and optimal data acquisition methods to increase the precision and accuracy of the measurements will be discussed. Finally, the extended application of isobaric labeling-based approach in hyperplexing strategy, targeted quantification, and phosphopeptide analysis are also examined.
引用
收藏
页码:5293 / 5309
页数:17
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