Statistical Inference from Multiple iTRAQ Experiments without Using Common Reference Standards

Shelley M. Herbrich(The University of Texas MD Anderson Cancer Center), Robert N. Cole(Johns Hopkins Medicine), Keith P. West(Johns Hopkins University), Kerry Schulze(Johns Hopkins University), James D. Yager(Johns Hopkins University), John D. Groopman(Johns Hopkins University), Parul Christian(Johns Hopkins University), Lee Wu(Johns Hopkins University), Robert N. O’Meally(Johns Hopkins University), Damon May(Fred Hutch Cancer Center), Martin McIntosh(Fred Hutch Cancer Center), Ingo Ruczinski(Johns Hopkins University)
Journal of Proteome Research
December 27, 2012
Cited by 143

Abstract

Isobaric tags for relative and absolute quantitation (iTRAQ) is a prominent mass spectrometry technology for protein identification and quantification that is capable of analyzing multiple samples in a single experiment. Frequently, iTRAQ experiments are carried out using an aliquot from a pool of all samples, or "masterpool", in one of the channels as a reference sample standard to estimate protein relative abundances in the biological samples and to combine abundance estimates from multiple experiments. In this manuscript, we show that using a masterpool is counterproductive. We obtain more precise estimates of protein relative abundance by using the available biological data instead of the masterpool and do not need to occupy a channel that could otherwise be used for another biological sample. In addition, we introduce a simple statistical method to associate proteomic data from multiple iTRAQ experiments with a numeric response and show that this approach is more powerful than the conventionally employed masterpool-based approach. We illustrate our methods using data from four replicate iTRAQ experiments on aliquots of the same pool of plasma samples and from a 406-sample project designed to identify plasma proteins that covary with nutrient concentrations in chronically undernourished children from South Asia.


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