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Systematic Comparison of Label-Free, Metabolic Labeling, and Isobaric Chemical Labeling for Quantitative Proteomics on LTQ Orbitrap Velos

Journal of Proteome Research · 2011 · Vol. 11(3) · pp. 1582–1590
Zhou LiRachel M. AdamsKaruna ChoureyGregory B. HurstRobert L. HettichChongle Pan

Abstract

A variety of quantitative proteomics methods have been developed, including label-free, metabolic labeling, and isobaric chemical labeling using iTRAQ or TMT. Here, these methods were compared in terms of the depth of proteome coverage, quantification accuracy, precision, and reproducibility using a high-performance hybrid mass spectrometer, LTQ Orbitrap Velos. Our results show that (1) the spectral counting method provides the deepest proteome coverage for identification, but its quantification performance is worse than labeling-based approaches, especially the quantification reproducibility; (2) metabolic labeling and isobaric chemical labeling are capable of accurate, precise, and reproducible quantification and provide deep proteome coverage for quantification; isobaric chemical labeling surpasses metabolic labeling in terms of quantification precision and reproducibility; and (3) iTRAQ and TMT perform similarly in all aspects compared in the current study using a CID-HCD dual scan configuration. On the basis of the unique advantages of each method, we provide guidance for selection of the appropriate method for a quantitative proteomics study.

Advanced Proteomics Techniques and ApplicationsMass Spectrometry Techniques and ApplicationsMetabolomics and Mass Spectrometry StudiesOrbitrapIsobaric labelingQuantitative proteomicsProteomeReproducibilityIsobaric processMass spectrometryChemistryLabel-free quantificationProteomics

MeSH terms

AlgorithmsBacterial ProteinsIsotope LabelingPeptide FragmentsPeptide MappingStaining and LabelingReproducibility of ResultsPseudomonas putidaProteomeProteomicsTandem Mass Spectrometry
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