iTRAQ reagent-based quantitative proteomic analysis on a linear ion trap mass spectrometer

被引:107
作者
Griffin, Timothy J.
Xie, Hongwei
Bandhakavi, Sricharan
Popko, Jonathan
Mohan, Archana
Carlis, John V.
Higgins, LeeAnn
机构
[1] Univ Minnesota, Dept Biochem Mol Biol & Biophys, Minneapolis, MN 55455 USA
[2] Univ Minnesota, Dept Comp Sci & Engn, Minneapolis, MN 55455 USA
[3] Univ Minnesota, Ctr Mass Spectrometry & Proteom, Minneapolis, MN 55455 USA
关键词
quantitative proteomics; iTRAQ; linear ion trap; pulsed-Q-dissociation;
D O I
10.1021/pr070291b
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
For proteomic analysis using tandem mass spectrometry, linear ion trap instruments provide unsurpassed sensitivity but unreliably detect low mass peptide fragments, precluding their use with iTRAQ reagent-labeled samples. Although the popular LTQ linear ion trap supports analyzing iTRAQ reagent-labeled peptides via pulsed Q dissociation, PQD, its effectiveness remains questionable. Using a standard mixture, we found careful tuning of relative collision energy necessary for fragmenting iTRAQ reagent-labeled peptides, and increasing microscan acquisition and repeat count improves quantification but identifies somewhat fewer peptides. We developed software to calculate abundance ratios via summing reporter ion intensities across spectra matching to each protein, thereby providing maximized accuracy. Testing found that results closely corresponded between analysis using optimized LTQ-PQD settings plus our software and using a Qstar instrument. Thus, we demonstrate the effectiveness of LTQ-PQD analyzing iTRAQ reagent-labeled peptides, and provide guidelines for successful quantitative proteomic studies.
引用
收藏
页码:4200 / 4209
页数:10
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