High Precision Quantitative Proteomics Using iTRAQ on an LTQ Orbitrap: A New Mass Spectrometric Method Combining the Benefits of All

Thomas Köcher(University of Vienna), Peter Pichler(Institute of Molecular Biotechnology), Michael Schutzbier(Institute of Molecular Biotechnology), Christoph Stingl(University of Vienna), Axel Kaul(Institute of Molecular Biotechnology), Nils Teucher(Research Institute of Molecular Pathology), Gerd Hasenfuß(University of Vienna), Josef Penninger(Research Institute of Molecular Pathology), Karl Mechtler(Research Institute of Molecular Pathology)
Journal of Proteome Research
August 11, 2009
Cited by 151Open Access
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Abstract

The development of quantitative techniques in mass spectrometry has generated the ability to systematically monitor protein expression. Isobaric tags for relative and absolute quantification (iTRAQ) have become a widely used tool for the quantification of proteins. However, application of iTRAQ methodology using ion traps and hybrid mass spectrometers containing an ion trap such as the LTQ-Orbitrap was not possible until the development of pulsed Q dissociation (PQD) and higher energy C-trap dissociation (HCD). Both methods allow iTRAQ-based quantification on an LTQ-Orbitrap but are less suited for protein identification at a proteomic scale than the commonly used collisional induced dissociation (CID) fragmentation. We developed an analytical strategy combining the advantages of CID and HCD, allowing sensitive and accurate protein identification and quantitation at the same time. In a direct comparison, the novel method outperformed PQD and HCD regarding its limit of detection, the number of identified peptides and the analytical precision of quantitation. The new method was applied to study changes in protein expression in mouse hearts upon transverse aortic constriction, a model for cardiac stress.


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