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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2015
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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. |
format | Online Article Text |
id | pubmed-4309027 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
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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