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Universal database search tool for proteomics

Mass spectrometry (MS) instruments and experimental protocols are rapidly advancing, but the software tools to analyze tandem mass spectra are lagging behind. We present a database search tool MS-GF+ that is sensitive (it identifies more peptides than most other database search tools) and universal...

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Detalles Bibliográficos
Autores principales: Kim, Sangtae, Pevzner, Pavel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036525/
https://www.ncbi.nlm.nih.gov/pubmed/25358478
http://dx.doi.org/10.1038/ncomms6277
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author Kim, Sangtae
Pevzner, Pavel A.
author_facet Kim, Sangtae
Pevzner, Pavel A.
author_sort Kim, Sangtae
collection PubMed
description Mass spectrometry (MS) instruments and experimental protocols are rapidly advancing, but the software tools to analyze tandem mass spectra are lagging behind. We present a database search tool MS-GF+ that is sensitive (it identifies more peptides than most other database search tools) and universal (it works well for diverse types of spectra, different configurations of MS instruments and different experimental protocols). We benchmark MS-GF+ using diverse spectral datasets: (i) spectra of varying fragmentation methods; (ii) spectra of multiple enzyme digests; (iii) spectra of phosphorylated peptides; (iv) spectra of peptides with unusual fragmentation propensities produced by a novel alpha-lytic protease. For all these datasets, MS-GF+ significantly increases the number of identified peptides compared to commonly used methods for peptide identifications. We emphasize that while MS-GF+ is not specifically designed for any particular experimental set-up, it improves upon the performance of tools specifically designed for these applications (e.g., specialized tools for phosphoproteomics).
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spelling pubmed-50365252016-09-26 Universal database search tool for proteomics Kim, Sangtae Pevzner, Pavel A. Nat Commun Article Mass spectrometry (MS) instruments and experimental protocols are rapidly advancing, but the software tools to analyze tandem mass spectra are lagging behind. We present a database search tool MS-GF+ that is sensitive (it identifies more peptides than most other database search tools) and universal (it works well for diverse types of spectra, different configurations of MS instruments and different experimental protocols). We benchmark MS-GF+ using diverse spectral datasets: (i) spectra of varying fragmentation methods; (ii) spectra of multiple enzyme digests; (iii) spectra of phosphorylated peptides; (iv) spectra of peptides with unusual fragmentation propensities produced by a novel alpha-lytic protease. For all these datasets, MS-GF+ significantly increases the number of identified peptides compared to commonly used methods for peptide identifications. We emphasize that while MS-GF+ is not specifically designed for any particular experimental set-up, it improves upon the performance of tools specifically designed for these applications (e.g., specialized tools for phosphoproteomics). 2014-10-31 /pmc/articles/PMC5036525/ /pubmed/25358478 http://dx.doi.org/10.1038/ncomms6277 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms
spellingShingle Article
Kim, Sangtae
Pevzner, Pavel A.
Universal database search tool for proteomics
title Universal database search tool for proteomics
title_full Universal database search tool for proteomics
title_fullStr Universal database search tool for proteomics
title_full_unstemmed Universal database search tool for proteomics
title_short Universal database search tool for proteomics
title_sort universal database search tool for proteomics
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5036525/
https://www.ncbi.nlm.nih.gov/pubmed/25358478
http://dx.doi.org/10.1038/ncomms6277
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