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Influence of Post-Translational Modifications on Protein Identification in Database Searches
[Image: see text] Comprehensive analysis of post-translation modifications (PTMs) is an important mission of proteomics. However, the consideration of PTMs increases the search space and may therefore impair the efficiency of protein identification. Using thousands of proteomic searches, we investig...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2021
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992065/ https://www.ncbi.nlm.nih.gov/pubmed/33778259 http://dx.doi.org/10.1021/acsomega.0c05997 |
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author | Bugyi, Fanni Szabó, Dániel Szabó, Győző Révész, Ágnes Pape, Veronika F. S. Soltész-Katona, Eszter Tóth, Eszter Kovács, Orsolya Langó, Tamás Vékey, Károly Drahos, László |
author_facet | Bugyi, Fanni Szabó, Dániel Szabó, Győző Révész, Ágnes Pape, Veronika F. S. Soltész-Katona, Eszter Tóth, Eszter Kovács, Orsolya Langó, Tamás Vékey, Károly Drahos, László |
author_sort | Bugyi, Fanni |
collection | PubMed |
description | [Image: see text] Comprehensive analysis of post-translation modifications (PTMs) is an important mission of proteomics. However, the consideration of PTMs increases the search space and may therefore impair the efficiency of protein identification. Using thousands of proteomic searches, we investigated the practical aspects of considering multiple PTMs in Byonic searches for the maximization of protein and peptide hits. The inclusion of all PTMs, which occur with at least 2% frequency in the sample, has an advantageous effect on protein and peptide identification. A linear relationship was established between the number of considered PTMs and the number of reliably identified peptides and proteins. Even though they handle multiple modifications less efficiently, the results of MASCOT (using the Percolator function) and Andromeda (the search engine included in MaxQuant) became comparable to those of Byonic, in the case of a few PTMs. |
format | Online Article Text |
id | pubmed-7992065 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-79920652021-03-26 Influence of Post-Translational Modifications on Protein Identification in Database Searches Bugyi, Fanni Szabó, Dániel Szabó, Győző Révész, Ágnes Pape, Veronika F. S. Soltész-Katona, Eszter Tóth, Eszter Kovács, Orsolya Langó, Tamás Vékey, Károly Drahos, László ACS Omega [Image: see text] Comprehensive analysis of post-translation modifications (PTMs) is an important mission of proteomics. However, the consideration of PTMs increases the search space and may therefore impair the efficiency of protein identification. Using thousands of proteomic searches, we investigated the practical aspects of considering multiple PTMs in Byonic searches for the maximization of protein and peptide hits. The inclusion of all PTMs, which occur with at least 2% frequency in the sample, has an advantageous effect on protein and peptide identification. A linear relationship was established between the number of considered PTMs and the number of reliably identified peptides and proteins. Even though they handle multiple modifications less efficiently, the results of MASCOT (using the Percolator function) and Andromeda (the search engine included in MaxQuant) became comparable to those of Byonic, in the case of a few PTMs. American Chemical Society 2021-03-15 /pmc/articles/PMC7992065/ /pubmed/33778259 http://dx.doi.org/10.1021/acsomega.0c05997 Text en © 2021 The Authors. Published by American Chemical Society Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Bugyi, Fanni Szabó, Dániel Szabó, Győző Révész, Ágnes Pape, Veronika F. S. Soltész-Katona, Eszter Tóth, Eszter Kovács, Orsolya Langó, Tamás Vékey, Károly Drahos, László Influence of Post-Translational Modifications on Protein Identification in Database Searches |
title | Influence of Post-Translational Modifications on Protein
Identification in Database Searches |
title_full | Influence of Post-Translational Modifications on Protein
Identification in Database Searches |
title_fullStr | Influence of Post-Translational Modifications on Protein
Identification in Database Searches |
title_full_unstemmed | Influence of Post-Translational Modifications on Protein
Identification in Database Searches |
title_short | Influence of Post-Translational Modifications on Protein
Identification in Database Searches |
title_sort | influence of post-translational modifications on protein
identification in database searches |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7992065/ https://www.ncbi.nlm.nih.gov/pubmed/33778259 http://dx.doi.org/10.1021/acsomega.0c05997 |
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