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Identification of modified peptides using localization-aware open search
Identification of post-translationally or chemically modified peptides in mass spectrometry-based proteomics experiments is a crucial yet challenging task. We have recently introduced a fragment ion indexing method and the MSFragger search engine to empower an open search strategy for comprehensive...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426425/ https://www.ncbi.nlm.nih.gov/pubmed/32792501 http://dx.doi.org/10.1038/s41467-020-17921-y |
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author | Yu, Fengchao Teo, Guo Ci Kong, Andy T. Haynes, Sarah E. Avtonomov, Dmitry M. Geiszler, Daniel J. Nesvizhskii, Alexey I. |
author_facet | Yu, Fengchao Teo, Guo Ci Kong, Andy T. Haynes, Sarah E. Avtonomov, Dmitry M. Geiszler, Daniel J. Nesvizhskii, Alexey I. |
author_sort | Yu, Fengchao |
collection | PubMed |
description | Identification of post-translationally or chemically modified peptides in mass spectrometry-based proteomics experiments is a crucial yet challenging task. We have recently introduced a fragment ion indexing method and the MSFragger search engine to empower an open search strategy for comprehensive analysis of modified peptides. However, this strategy does not consider fragment ions shifted by unknown modifications, preventing modification localization and limiting the sensitivity of the search. Here we present a localization-aware open search method, in which both modification-containing (shifted) and regular fragment ions are indexed and used in scoring. We also implement a fast mass calibration and optimization method, allowing optimization of the mass tolerances and other key search parameters. We demonstrate that MSFragger with mass calibration and localization-aware open search identifies modified peptides with significantly higher sensitivity and accuracy. Comparing MSFragger to other modification-focused tools (pFind3, MetaMorpheus, and TagGraph) shows that MSFragger remains an excellent option for fast, comprehensive, and sensitive searches for modified peptides in shotgun proteomics data. |
format | Online Article Text |
id | pubmed-7426425 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-74264252020-08-18 Identification of modified peptides using localization-aware open search Yu, Fengchao Teo, Guo Ci Kong, Andy T. Haynes, Sarah E. Avtonomov, Dmitry M. Geiszler, Daniel J. Nesvizhskii, Alexey I. Nat Commun Article Identification of post-translationally or chemically modified peptides in mass spectrometry-based proteomics experiments is a crucial yet challenging task. We have recently introduced a fragment ion indexing method and the MSFragger search engine to empower an open search strategy for comprehensive analysis of modified peptides. However, this strategy does not consider fragment ions shifted by unknown modifications, preventing modification localization and limiting the sensitivity of the search. Here we present a localization-aware open search method, in which both modification-containing (shifted) and regular fragment ions are indexed and used in scoring. We also implement a fast mass calibration and optimization method, allowing optimization of the mass tolerances and other key search parameters. We demonstrate that MSFragger with mass calibration and localization-aware open search identifies modified peptides with significantly higher sensitivity and accuracy. Comparing MSFragger to other modification-focused tools (pFind3, MetaMorpheus, and TagGraph) shows that MSFragger remains an excellent option for fast, comprehensive, and sensitive searches for modified peptides in shotgun proteomics data. Nature Publishing Group UK 2020-08-13 /pmc/articles/PMC7426425/ /pubmed/32792501 http://dx.doi.org/10.1038/s41467-020-17921-y Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yu, Fengchao Teo, Guo Ci Kong, Andy T. Haynes, Sarah E. Avtonomov, Dmitry M. Geiszler, Daniel J. Nesvizhskii, Alexey I. Identification of modified peptides using localization-aware open search |
title | Identification of modified peptides using localization-aware open search |
title_full | Identification of modified peptides using localization-aware open search |
title_fullStr | Identification of modified peptides using localization-aware open search |
title_full_unstemmed | Identification of modified peptides using localization-aware open search |
title_short | Identification of modified peptides using localization-aware open search |
title_sort | identification of modified peptides using localization-aware open search |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7426425/ https://www.ncbi.nlm.nih.gov/pubmed/32792501 http://dx.doi.org/10.1038/s41467-020-17921-y |
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