iTRAQ protein quantification: A quality-controlled workflow

被引:43
|
作者
Burkhart, Julia M. [1 ]
Vaudel, Marc [1 ]
Zahedi, Rene P. [1 ]
Martens, Lennart [2 ,3 ]
Sickmann, Albert [1 ,4 ]
机构
[1] Leibniz Inst Analyt Wissensch ISAS eV, D-44227 Dortmund, Germany
[2] VIB, Dept Med Prot Res, Ghent, Belgium
[3] Univ Ghent, Dept Biochem, B-9000 Ghent, Belgium
[4] Ruhr Univ Bochum, Med Proteom Ctr MPC, Bochum, Germany
关键词
iTRAQ; Mass spectrometry; Quantification; Technology; MASS-SPECTROMETRY; ABSOLUTE QUANTIFICATION; COMPARATIVE PROTEOMICS; ISOBARIC TAGS; PEPTIDE; IDENTIFICATION; DATABASES; ABUNDANCE; STRATEGY; ORBITRAP;
D O I
10.1002/pmic.201000711
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Reporter ion-based methods are among the major techniques to quantify peptides and proteins. Two main labels, tandem mass tag (TMT) and iTRAQ, are widely used by the proteomics community. They are, however, often applied as out-of-the-box methods, without thorough quality control. Thus, due to undiscovered limitations of the technique, irrelevant results might be trusted. To address this issue, we here propose a step-by-step quality control of the iTRAQ workflow. From sample preparation to final ratio calculation we provide metrics and techniques assessing the actual effectiveness of iTRAQ quantification as well as a novel method for more reliable protein ratio estimation.
引用
收藏
页码:1125 / 1134
页数:10
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