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Prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry

Motivation: Complex patterns of protein phosphorylation mediate many cellular processes. Tandem mass spectrometry (MS/MS) is a powerful tool for identifying these post-translational modifications. In high-throughput experiments, mass spectrometry database search engines, such as MASCOT provide a ran...

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Autores principales: Martin, David M.A., Nett, Isabelle R.E., Vandermoere, Franck, Barber, Jonathan D., Morrice, Nicholas A., Ferguson, Michael A.J.
Formato: Texto
Lenguaje:English
Publicado: Oxford University Press 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2922888/
https://www.ncbi.nlm.nih.gov/pubmed/20651112
http://dx.doi.org/10.1093/bioinformatics/btq341
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author Martin, David M.A.
Nett, Isabelle R.E.
Vandermoere, Franck
Barber, Jonathan D.
Morrice, Nicholas A.
Ferguson, Michael A.J.
author_facet Martin, David M.A.
Nett, Isabelle R.E.
Vandermoere, Franck
Barber, Jonathan D.
Morrice, Nicholas A.
Ferguson, Michael A.J.
author_sort Martin, David M.A.
collection PubMed
description Motivation: Complex patterns of protein phosphorylation mediate many cellular processes. Tandem mass spectrometry (MS/MS) is a powerful tool for identifying these post-translational modifications. In high-throughput experiments, mass spectrometry database search engines, such as MASCOT provide a ranked list of peptide identifications based on hundreds of thousands of MS/MS spectra obtained in a mass spectrometry experiment. These search results are not in themselves sufficient for confident assignment of phosphorylation sites as identification of characteristic mass differences requires time-consuming manual assessment of the spectra by an experienced analyst. The time required for manual assessment has previously rendered high-throughput confident assignment of phosphorylation sites challenging. Results: We have developed a knowledge base of criteria, which replicate expert assessment, allowing more than half of cases to be automatically validated and site assignments verified with a high degree of confidence. This was assessed by comparing automated spectral interpretation with careful manual examination of the assignments for 501 peptides above the 1% false discovery rate (FDR) threshold corresponding to 259 putative phosphorylation sites in 74 proteins of the Trypanosoma brucei proteome. Despite this stringent approach, we are able to validate 80 of the 91 phosphorylation sites (88%) positively identified by manual examination of the spectra used for the MASCOT searches with a FDR < 15%. Conclusions:High-throughput computational analysis can provide a viable second stage validation of primary mass spectrometry database search results. Such validation gives rapid access to a systems level overview of protein phosphorylation in the experiment under investigation. Availability: A GPL licensed software implementation in Perl for analysis and spectrum annotation is available in the supplementary material and a web server can be assessed online at http://www.compbio.dundee.ac.uk/prophossi Contact: d.m.a.martin@dundee.ac.uk Supplementary information: Supplementary data are available at Bioinformatics online.
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spelling pubmed-29228882010-08-30 Prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry Martin, David M.A. Nett, Isabelle R.E. Vandermoere, Franck Barber, Jonathan D. Morrice, Nicholas A. Ferguson, Michael A.J. Bioinformatics Original Papers Motivation: Complex patterns of protein phosphorylation mediate many cellular processes. Tandem mass spectrometry (MS/MS) is a powerful tool for identifying these post-translational modifications. In high-throughput experiments, mass spectrometry database search engines, such as MASCOT provide a ranked list of peptide identifications based on hundreds of thousands of MS/MS spectra obtained in a mass spectrometry experiment. These search results are not in themselves sufficient for confident assignment of phosphorylation sites as identification of characteristic mass differences requires time-consuming manual assessment of the spectra by an experienced analyst. The time required for manual assessment has previously rendered high-throughput confident assignment of phosphorylation sites challenging. Results: We have developed a knowledge base of criteria, which replicate expert assessment, allowing more than half of cases to be automatically validated and site assignments verified with a high degree of confidence. This was assessed by comparing automated spectral interpretation with careful manual examination of the assignments for 501 peptides above the 1% false discovery rate (FDR) threshold corresponding to 259 putative phosphorylation sites in 74 proteins of the Trypanosoma brucei proteome. Despite this stringent approach, we are able to validate 80 of the 91 phosphorylation sites (88%) positively identified by manual examination of the spectra used for the MASCOT searches with a FDR < 15%. Conclusions:High-throughput computational analysis can provide a viable second stage validation of primary mass spectrometry database search results. Such validation gives rapid access to a systems level overview of protein phosphorylation in the experiment under investigation. Availability: A GPL licensed software implementation in Perl for analysis and spectrum annotation is available in the supplementary material and a web server can be assessed online at http://www.compbio.dundee.ac.uk/prophossi Contact: d.m.a.martin@dundee.ac.uk Supplementary information: Supplementary data are available at Bioinformatics online. Oxford University Press 2010-09-01 2010-07-22 /pmc/articles/PMC2922888/ /pubmed/20651112 http://dx.doi.org/10.1093/bioinformatics/btq341 Text en © The Author(s) 2010. Published by Oxford University Press. http://creativecommons.org/licenses/by-nc/2.0/uk/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/2.5), which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Papers
Martin, David M.A.
Nett, Isabelle R.E.
Vandermoere, Franck
Barber, Jonathan D.
Morrice, Nicholas A.
Ferguson, Michael A.J.
Prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry
title Prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry
title_full Prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry
title_fullStr Prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry
title_full_unstemmed Prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry
title_short Prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry
title_sort prophossi: automating expert validation of phosphopeptide–spectrum matches from tandem mass spectrometry
topic Original Papers
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2922888/
https://www.ncbi.nlm.nih.gov/pubmed/20651112
http://dx.doi.org/10.1093/bioinformatics/btq341
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