A new strategy for MS/MS data acquisition applying multiple data dependent experiments on Orbitrap mass spectrometers in non-targeted metabolomic applications

The annotation and identification of metabolites is a current bottleneck in non-targeted metabolomics studies. Although accurate measurement of m/z is applied routinely in UPLC–MS applications to putatively annotate metabolites, the acquisition of MS/MS or MS n data is required to deduce structural...

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Veröffentlicht in:Metabolomics 2015-10, Vol.11 (5), p.1068-1080
Hauptverfasser: Mullard, Graham, Allwood, James W., Weber, Ralf, Brown, Marie, Begley, Paul, Hollywood, Katherine A., Jones, Martin, Unwin, Richard D., Bishop, Paul N., Cooper, Garth J. S., Dunn, Warwick B.
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container_end_page 1080
container_issue 5
container_start_page 1068
container_title Metabolomics
container_volume 11
creator Mullard, Graham
Allwood, James W.
Weber, Ralf
Brown, Marie
Begley, Paul
Hollywood, Katherine A.
Jones, Martin
Unwin, Richard D.
Bishop, Paul N.
Cooper, Garth J. S.
Dunn, Warwick B.
description The annotation and identification of metabolites is a current bottleneck in non-targeted metabolomics studies. Although accurate measurement of m/z is applied routinely in UPLC–MS applications to putatively annotate metabolites, the acquisition of MS/MS or MS n data is required to deduce structural information, further reducing the chemical search-space and providing greater confidence in metabolite annotation by comparison to mass spectral databases. Here we propose an innovative new strategy for data dependent acquisition (DDA) for on-line MS/MS data acquisition in parallel to full-scan metabolite profiling on LTQ-Orbitrap mass spectrometers. We recommend the application of different and integrated DDA MS/MS experiments to increase the coverage of unique metabolites for which MS/MS data were acquired. We demonstrate, for the first time, that the integrated application of both CID and higher-energy collisional dissociation ion activation methods, multiple different activation energies and narrow precursor ion m/z ranges of 100 or 300 for acquisition of MS/MS spectra provide complementary information and increases the number of unique metabolites for which MS/MS data is acquired. The strategies herein provide a different approach for data acquisition to increase the number of unique MS/MS mass spectra acquired for metabolite annotation purposes in non-targeted metabolomics studies. MS/MS data are available on request from the corresponding author.
doi_str_mv 10.1007/s11306-014-0763-6
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subjects Biochemistry
Biomedical and Life Sciences
Biomedicine
Cell Biology
Developmental Biology
Life Sciences
Molecular Medicine
Original Article
title A new strategy for MS/MS data acquisition applying multiple data dependent experiments on Orbitrap mass spectrometers in non-targeted metabolomic applications
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