Cargando…
Cleaning out the Litterbox of Proteomic Scientists’ Favorite Pet: Optimized Data Analysis Avoiding Trypsin Artifacts
[Image: see text] Chemically modified trypsin is a standard reagent in proteomics experiments but is usually not considered in database searches. Modification of trypsin is supposed to protect the protease against autolysis and the resulting loss of activity. Here, we show that modified trypsin is s...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2016
|
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820788/ https://www.ncbi.nlm.nih.gov/pubmed/26938934 http://dx.doi.org/10.1021/acs.jproteome.5b01105 |
_version_ | 1782425470555389952 |
---|---|
author | Schittmayer, Matthias Fritz, Katarina Liesinger, Laura Griss, Johannes Birner-Gruenberger, Ruth |
author_facet | Schittmayer, Matthias Fritz, Katarina Liesinger, Laura Griss, Johannes Birner-Gruenberger, Ruth |
author_sort | Schittmayer, Matthias |
collection | PubMed |
description | [Image: see text] Chemically modified trypsin is a standard reagent in proteomics experiments but is usually not considered in database searches. Modification of trypsin is supposed to protect the protease against autolysis and the resulting loss of activity. Here, we show that modified trypsin is still subject to self-digestion, and, as a result, modified trypsin-derived peptides are present in standard digests. We depict that these peptides commonly lead to false-positive assignments even if native trypsin is considered in the database. Moreover, we present an easily implementable method to include modified trypsin in the database search with a minimal increase in search time and search space while efficiently avoiding these false-positive hits. |
format | Online Article Text |
id | pubmed-4820788 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-48207882016-04-06 Cleaning out the Litterbox of Proteomic Scientists’ Favorite Pet: Optimized Data Analysis Avoiding Trypsin Artifacts Schittmayer, Matthias Fritz, Katarina Liesinger, Laura Griss, Johannes Birner-Gruenberger, Ruth J Proteome Res [Image: see text] Chemically modified trypsin is a standard reagent in proteomics experiments but is usually not considered in database searches. Modification of trypsin is supposed to protect the protease against autolysis and the resulting loss of activity. Here, we show that modified trypsin is still subject to self-digestion, and, as a result, modified trypsin-derived peptides are present in standard digests. We depict that these peptides commonly lead to false-positive assignments even if native trypsin is considered in the database. Moreover, we present an easily implementable method to include modified trypsin in the database search with a minimal increase in search time and search space while efficiently avoiding these false-positive hits. American Chemical Society 2016-03-03 2016-04-01 /pmc/articles/PMC4820788/ /pubmed/26938934 http://dx.doi.org/10.1021/acs.jproteome.5b01105 Text en Copyright © 2016 American Chemical Society This is an open access article published under a Creative Commons Attribution (CC-BY) License (http://pubs.acs.org/page/policy/authorchoice_ccby_termsofuse.html) , which permits unrestricted use, distribution and reproduction in any medium, provided the author and source are cited. |
spellingShingle | Schittmayer, Matthias Fritz, Katarina Liesinger, Laura Griss, Johannes Birner-Gruenberger, Ruth Cleaning out the Litterbox of Proteomic Scientists’ Favorite Pet: Optimized Data Analysis Avoiding Trypsin Artifacts |
title | Cleaning out the
Litterbox of Proteomic Scientists’
Favorite Pet: Optimized Data Analysis Avoiding Trypsin Artifacts |
title_full | Cleaning out the
Litterbox of Proteomic Scientists’
Favorite Pet: Optimized Data Analysis Avoiding Trypsin Artifacts |
title_fullStr | Cleaning out the
Litterbox of Proteomic Scientists’
Favorite Pet: Optimized Data Analysis Avoiding Trypsin Artifacts |
title_full_unstemmed | Cleaning out the
Litterbox of Proteomic Scientists’
Favorite Pet: Optimized Data Analysis Avoiding Trypsin Artifacts |
title_short | Cleaning out the
Litterbox of Proteomic Scientists’
Favorite Pet: Optimized Data Analysis Avoiding Trypsin Artifacts |
title_sort | cleaning out the
litterbox of proteomic scientists’
favorite pet: optimized data analysis avoiding trypsin artifacts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4820788/ https://www.ncbi.nlm.nih.gov/pubmed/26938934 http://dx.doi.org/10.1021/acs.jproteome.5b01105 |
work_keys_str_mv | AT schittmayermatthias cleaningoutthelitterboxofproteomicscientistsfavoritepetoptimizeddataanalysisavoidingtrypsinartifacts AT fritzkatarina cleaningoutthelitterboxofproteomicscientistsfavoritepetoptimizeddataanalysisavoidingtrypsinartifacts AT liesingerlaura cleaningoutthelitterboxofproteomicscientistsfavoritepetoptimizeddataanalysisavoidingtrypsinartifacts AT grissjohannes cleaningoutthelitterboxofproteomicscientistsfavoritepetoptimizeddataanalysisavoidingtrypsinartifacts AT birnergruenbergerruth cleaningoutthelitterboxofproteomicscientistsfavoritepetoptimizeddataanalysisavoidingtrypsinartifacts |