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PhosphoHunter: An Efficient Software Tool for Phosphopeptide Identification

Phosphorylation is a protein posttranslational modification. It is responsible of the activation/inactivation of disease-related pathways, thanks to its role of “molecular switch.” The study of phosphorylated proteins becomes a key point for the proteomic analyses focused on the identification of di...

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Detalles Bibliográficos
Autores principales: Tiengo, Alessandra, Pasotti, Lorenzo, Barbarini, Nicola, Magni, Paolo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309027/
https://www.ncbi.nlm.nih.gov/pubmed/25653679
http://dx.doi.org/10.1155/2015/382869
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author Tiengo, Alessandra
Pasotti, Lorenzo
Barbarini, Nicola
Magni, Paolo
author_facet Tiengo, Alessandra
Pasotti, Lorenzo
Barbarini, Nicola
Magni, Paolo
author_sort Tiengo, Alessandra
collection PubMed
description Phosphorylation is a protein posttranslational modification. It is responsible of the activation/inactivation of disease-related pathways, thanks to its role of “molecular switch.” The study of phosphorylated proteins becomes a key point for the proteomic analyses focused on the identification of diagnostic/therapeutic targets. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) is the most widely used analytical approach. Although unmodified peptides are automatically identified by consolidated algorithms, phosphopeptides still require automated tools to avoid time-consuming manual interpretation. To improve phosphopeptide identification efficiency, a novel procedure was developed and implemented in a Perl/C tool called PhosphoHunter, here proposed and evaluated. It includes a preliminary heuristic step for filtering out the MS/MS spectra produced by nonphosphorylated peptides before sequence identification. A method to assess the statistical significance of identified phosphopeptides was also formulated. PhosphoHunter performance was tested on a dataset of 1500 MS/MS spectra and it was compared with two other tools: Mascot and Inspect. Comparisons demonstrated that a strong point of PhosphoHunter is sensitivity, suggesting that it is able to identify real phosphopeptides with superior performance. Performance indexes depend on a single parameter (intensity threshold) that users can tune according to the study aim. All the three tools localized >90% of phosphosites.
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spelling pubmed-43090272015-02-04 PhosphoHunter: An Efficient Software Tool for Phosphopeptide Identification Tiengo, Alessandra Pasotti, Lorenzo Barbarini, Nicola Magni, Paolo Adv Bioinformatics Research Article Phosphorylation is a protein posttranslational modification. It is responsible of the activation/inactivation of disease-related pathways, thanks to its role of “molecular switch.” The study of phosphorylated proteins becomes a key point for the proteomic analyses focused on the identification of diagnostic/therapeutic targets. Liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS) is the most widely used analytical approach. Although unmodified peptides are automatically identified by consolidated algorithms, phosphopeptides still require automated tools to avoid time-consuming manual interpretation. To improve phosphopeptide identification efficiency, a novel procedure was developed and implemented in a Perl/C tool called PhosphoHunter, here proposed and evaluated. It includes a preliminary heuristic step for filtering out the MS/MS spectra produced by nonphosphorylated peptides before sequence identification. A method to assess the statistical significance of identified phosphopeptides was also formulated. PhosphoHunter performance was tested on a dataset of 1500 MS/MS spectra and it was compared with two other tools: Mascot and Inspect. Comparisons demonstrated that a strong point of PhosphoHunter is sensitivity, suggesting that it is able to identify real phosphopeptides with superior performance. Performance indexes depend on a single parameter (intensity threshold) that users can tune according to the study aim. All the three tools localized >90% of phosphosites. Hindawi Publishing Corporation 2015 2015-01-12 /pmc/articles/PMC4309027/ /pubmed/25653679 http://dx.doi.org/10.1155/2015/382869 Text en Copyright © 2015 Alessandra Tiengo et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Tiengo, Alessandra
Pasotti, Lorenzo
Barbarini, Nicola
Magni, Paolo
PhosphoHunter: An Efficient Software Tool for Phosphopeptide Identification
title PhosphoHunter: An Efficient Software Tool for Phosphopeptide Identification
title_full PhosphoHunter: An Efficient Software Tool for Phosphopeptide Identification
title_fullStr PhosphoHunter: An Efficient Software Tool for Phosphopeptide Identification
title_full_unstemmed PhosphoHunter: An Efficient Software Tool for Phosphopeptide Identification
title_short PhosphoHunter: An Efficient Software Tool for Phosphopeptide Identification
title_sort phosphohunter: an efficient software tool for phosphopeptide identification
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4309027/
https://www.ncbi.nlm.nih.gov/pubmed/25653679
http://dx.doi.org/10.1155/2015/382869
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