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MS Annika 2.0 Identifies Cross-Linked Peptides in MS2–MS3-Based Workflows at High Sensitivity and Specificity

[Image: see text] Cross-linking mass spectrometry has become a powerful tool for the identification of protein–protein interactions and for gaining insight into the structures of proteins. We previously published MS Annika, a cross-linking search engine which can accurately identify cross-linked pep...

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Autores principales: Birklbauer, Micha J., Matzinger, Manuel, Müller, Fränze, Mechtler, Karl, Dorfer, Viktoria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2023
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476269/
https://www.ncbi.nlm.nih.gov/pubmed/37566781
http://dx.doi.org/10.1021/acs.jproteome.3c00325
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author Birklbauer, Micha J.
Matzinger, Manuel
Müller, Fränze
Mechtler, Karl
Dorfer, Viktoria
author_facet Birklbauer, Micha J.
Matzinger, Manuel
Müller, Fränze
Mechtler, Karl
Dorfer, Viktoria
author_sort Birklbauer, Micha J.
collection PubMed
description [Image: see text] Cross-linking mass spectrometry has become a powerful tool for the identification of protein–protein interactions and for gaining insight into the structures of proteins. We previously published MS Annika, a cross-linking search engine which can accurately identify cross-linked peptides in MS2 spectra from a variety of different MS-cleavable cross-linkers. In this publication, we present MS Annika 2.0, an updated version implementing a new search algorithm that, in addition to MS2 level, only supports the processing of data from MS2–MS3-based approaches for the identification of peptides from MS3 spectra, and introduces a novel scoring function for peptides identified across multiple MS stages. Detected cross-links are validated by estimating the false discovery rate (FDR) using a target-decoy approach. We evaluated the MS3-search-capabilities of MS Annika 2.0 on five different datasets covering a variety of experimental approaches and compared it to XlinkX and MaXLinker, two other cross-linking search engines. We show that MS Annika detects up to 4 times more true unique cross-links while simultaneously yielding less false positive hits and therefore a more accurate FDR estimation than the other two search engines. All mass spectrometry proteomics data along with result files have been deposited to the ProteomeXchange consortium via the PRIDE partner repository with the dataset identifier PXD041955.
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spelling pubmed-104762692023-09-05 MS Annika 2.0 Identifies Cross-Linked Peptides in MS2–MS3-Based Workflows at High Sensitivity and Specificity Birklbauer, Micha J. Matzinger, Manuel Müller, Fränze Mechtler, Karl Dorfer, Viktoria J Proteome Res [Image: see text] Cross-linking mass spectrometry has become a powerful tool for the identification of protein–protein interactions and for gaining insight into the structures of proteins. We previously published MS Annika, a cross-linking search engine which can accurately identify cross-linked peptides in MS2 spectra from a variety of different MS-cleavable cross-linkers. In this publication, we present MS Annika 2.0, an updated version implementing a new search algorithm that, in addition to MS2 level, only supports the processing of data from MS2–MS3-based approaches for the identification of peptides from MS3 spectra, and introduces a novel scoring function for peptides identified across multiple MS stages. Detected cross-links are validated by estimating the false discovery rate (FDR) using a target-decoy approach. We evaluated the MS3-search-capabilities of MS Annika 2.0 on five different datasets covering a variety of experimental approaches and compared it to XlinkX and MaXLinker, two other cross-linking search engines. We show that MS Annika detects up to 4 times more true unique cross-links while simultaneously yielding less false positive hits and therefore a more accurate FDR estimation than the other two search engines. All mass spectrometry proteomics data along with result files have been deposited to the ProteomeXchange consortium via the PRIDE partner repository with the dataset identifier PXD041955. American Chemical Society 2023-08-11 /pmc/articles/PMC10476269/ /pubmed/37566781 http://dx.doi.org/10.1021/acs.jproteome.3c00325 Text en © 2023 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by/4.0/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 Birklbauer, Micha J.
Matzinger, Manuel
Müller, Fränze
Mechtler, Karl
Dorfer, Viktoria
MS Annika 2.0 Identifies Cross-Linked Peptides in MS2–MS3-Based Workflows at High Sensitivity and Specificity
title MS Annika 2.0 Identifies Cross-Linked Peptides in MS2–MS3-Based Workflows at High Sensitivity and Specificity
title_full MS Annika 2.0 Identifies Cross-Linked Peptides in MS2–MS3-Based Workflows at High Sensitivity and Specificity
title_fullStr MS Annika 2.0 Identifies Cross-Linked Peptides in MS2–MS3-Based Workflows at High Sensitivity and Specificity
title_full_unstemmed MS Annika 2.0 Identifies Cross-Linked Peptides in MS2–MS3-Based Workflows at High Sensitivity and Specificity
title_short MS Annika 2.0 Identifies Cross-Linked Peptides in MS2–MS3-Based Workflows at High Sensitivity and Specificity
title_sort ms annika 2.0 identifies cross-linked peptides in ms2–ms3-based workflows at high sensitivity and specificity
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10476269/
https://www.ncbi.nlm.nih.gov/pubmed/37566781
http://dx.doi.org/10.1021/acs.jproteome.3c00325
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