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A synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes

Crosslinking-mass spectrometry (XL-MS) serves to identify interaction sites between proteins. Numerous search engines for crosslink identification exist, but lack of ground truth samples containing known crosslinks has precluded their systematic validation. Here we report on XL-MS data arising from...

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Autores principales: Beveridge, Rebecca, Stadlmann, Johannes, Penninger, Josef M., Mechtler, Karl
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005041/
https://www.ncbi.nlm.nih.gov/pubmed/32029734
http://dx.doi.org/10.1038/s41467-020-14608-2
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author Beveridge, Rebecca
Stadlmann, Johannes
Penninger, Josef M.
Mechtler, Karl
author_facet Beveridge, Rebecca
Stadlmann, Johannes
Penninger, Josef M.
Mechtler, Karl
author_sort Beveridge, Rebecca
collection PubMed
description Crosslinking-mass spectrometry (XL-MS) serves to identify interaction sites between proteins. Numerous search engines for crosslink identification exist, but lack of ground truth samples containing known crosslinks has precluded their systematic validation. Here we report on XL-MS data arising from measuring synthetic peptide libraries that provide the unique benefit of knowing which identified crosslinks are true and which are false. The data are analysed with the most frequently used search engines and the results filtered to an estimated false discovery rate of 5%. We find that the actual false crosslink identification rates range from 2.4 to 32%, depending on the analysis strategy employed. Furthermore, the use of MS-cleavable crosslinkers does not reduce the false discovery rate compared to non-cleavable crosslinkers. We anticipate that the datasets acquired during this research will further drive optimisation and development of XL-MS search engines, thereby advancing our understanding of vital biological interactions.
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spelling pubmed-70050412020-02-10 A synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes Beveridge, Rebecca Stadlmann, Johannes Penninger, Josef M. Mechtler, Karl Nat Commun Article Crosslinking-mass spectrometry (XL-MS) serves to identify interaction sites between proteins. Numerous search engines for crosslink identification exist, but lack of ground truth samples containing known crosslinks has precluded their systematic validation. Here we report on XL-MS data arising from measuring synthetic peptide libraries that provide the unique benefit of knowing which identified crosslinks are true and which are false. The data are analysed with the most frequently used search engines and the results filtered to an estimated false discovery rate of 5%. We find that the actual false crosslink identification rates range from 2.4 to 32%, depending on the analysis strategy employed. Furthermore, the use of MS-cleavable crosslinkers does not reduce the false discovery rate compared to non-cleavable crosslinkers. We anticipate that the datasets acquired during this research will further drive optimisation and development of XL-MS search engines, thereby advancing our understanding of vital biological interactions. Nature Publishing Group UK 2020-02-06 /pmc/articles/PMC7005041/ /pubmed/32029734 http://dx.doi.org/10.1038/s41467-020-14608-2 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
Beveridge, Rebecca
Stadlmann, Johannes
Penninger, Josef M.
Mechtler, Karl
A synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes
title A synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes
title_full A synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes
title_fullStr A synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes
title_full_unstemmed A synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes
title_short A synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes
title_sort synthetic peptide library for benchmarking crosslinking-mass spectrometry search engines for proteins and protein complexes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7005041/
https://www.ncbi.nlm.nih.gov/pubmed/32029734
http://dx.doi.org/10.1038/s41467-020-14608-2
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