A Data Processing Pipeline for Mammalian Proteome Dynamics Studies Using Stable Isotope Metabolic Labeling

In a recent study, in vivo metabolic labeling using 15N traced the rate of label incorporation among more than 1700 proteins simultaneously and enabled the determination of individual protein turnover rate constants over a dynamic range of three orders of magnitude (Price, J. C., Guan, S., Burlingam...

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Veröffentlicht in:Molecular & cellular proteomics 2011-12, Vol.10 (12), p.M111.010728-M111.010728, Article M111.010728
Hauptverfasser: Guan, Shenheng, Price, John C., Prusiner, Stanley B., Ghaemmaghami, Sina, Burlingame, Alma L.
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Sprache:eng
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Zusammenfassung:In a recent study, in vivo metabolic labeling using 15N traced the rate of label incorporation among more than 1700 proteins simultaneously and enabled the determination of individual protein turnover rate constants over a dynamic range of three orders of magnitude (Price, J. C., Guan, S., Burlingame, A., Prusiner, S. B., and Ghaemmaghami, S. (2010) Analysis of proteome dynamics in the mouse brain. Proc. Natl. Acad. Sci. U. S. A. 107, 14508–14513). These studies of protein dynamics provide a deeper understanding of healthy development and well-being of complex organisms, as well as the possible causes and progression of disease. In addition to a fully labeled food source and appropriate mass spectrometry platform, an essential and enabling component of such large scale investigations is a robust data processing and analysis pipeline, which is capable of the reduction of large sets of liquid chromatography tandem MS raw data files into the desired protein turnover rate constants. The data processing pipeline described in this contribution is comprised of a suite of software modules required for the workflow that fulfills such requirements. This software platform includes established software tools such as a mass spectrometry database search engine together with several additional, novel data processing modules specifically developed for 15N metabolic labeling. These fulfill the following functions: (1) cross-extraction of 15N-containing ion intensities from raw data files at varying biosynthetic incorporation times, (2) computation of peptide 15N isotopic incorporation distributions, and (3) aggregation of relative isotope abundance curves for multiple peptides into single protein curves. In addition, processing parameter optimization and noise reduction procedures were found to be necessary in the processing modules in order to reduce propagation of errors in the long chain of the processing steps of the entire workflow.
ISSN:1535-9476
1535-9484
DOI:10.1074/mcp.M111.010728