Abstract

BackgroundIsobaric Tags for Relative and Absolute Quantitation (iTRAQ™) [Applied Biosystems] have seen increased application in differential protein expression analysis. To facilitate the growing need to analyze iTRAQ data, especially for cases involving multiple iTRAQ experiments, we have developed a modeling approach, statistical methods, and tools for estimating the relative changes in protein expression under various treatments and experimental conditions.ResultsThis modeling approach provides a unified analysis of data from multiple iTRAQ experiments and links the observed quantity (reporter ion peak area) to the experiment design and the calculated quantity of interest (treatment-dependent protein and peptide fold change) through an additive model under log transformation. Others have demonstrated, through a case study, this modeling approach and noted the computational challenges of parameter inference in the unbalanced data set typical of multiple iTRAQ experiments. Here we present the development of an inference approach, based on hierarchical regression with batching of regression coefficients and Markov Chain Monte Carlo (MCMC) methods that overcomes some of these challenges. In addition to our discussion of the underlying method, we also present our implementation of the software, simulation results, experimental results, and sample output from the resulting analysis report.ConclusioniQuantitator's process-based modeling approach overcomes limitations in current methods and allows for application in a variety of experimental designs. Additionally, hypertext-linked documents produced by the tool aid in the interpretation and exploration of results.

Highlights

  • Isobaric Tags for Relative and Absolute Quantitation [Applied Biosystems] have seen increased application in differential protein expression analysis

  • Reagents, and techniques for high throughput proteomics are making it possible to simultaneously identify and compare disease, development, and treatment-related changes to the level of protein expression [1]. These techniques rely on two dimensional gel electrophoresis (2DGE) or liquid chromatography (LC) to separate proteins or peptides by charge, mass, or other chemical properties followed by identification using mass spectrometry (MS)

  • Simulated Data We find that the model-based approach implemented here results in a smaller mean square error in the estimated log fold changes when compared to individual paired estimates using the log averaging approach or when those paired estimates are averaged

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Summary

Introduction

Isobaric Tags for Relative and Absolute Quantitation (iTRAQTM) [Applied Biosystems] have seen increased application in differential protein expression analysis. Reagents, and techniques for high throughput proteomics are making it possible to simultaneously identify and compare disease, development, and treatment-related changes to the level of protein expression [1]. In most cases, these techniques rely on two dimensional gel electrophoresis (2DGE) or liquid chromatography (LC) to separate proteins or peptides by charge, mass, or other chemical properties followed by identification using mass spectrometry (MS). The methods compute protein abundance indices from the average of the associated peptide abundances based on these frequencies

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