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FLASHIda enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts
The detailed analysis and structural characterization of proteoforms by top-down proteomics (TDP) has gained a lot of interest in biomedical research. Data-dependent acquisition (DDA) of intact proteins is non-trivial due to the diversity and complexity of proteoforms. Dedicated acquisition methods...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338294/ https://www.ncbi.nlm.nih.gov/pubmed/35906205 http://dx.doi.org/10.1038/s41467-022-31922-z |
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author | Jeong, Kyowon Babović, Maša Gorshkov, Vladimir Kim, Jihyung Jensen, Ole N. Kohlbacher, Oliver |
author_facet | Jeong, Kyowon Babović, Maša Gorshkov, Vladimir Kim, Jihyung Jensen, Ole N. Kohlbacher, Oliver |
author_sort | Jeong, Kyowon |
collection | PubMed |
description | The detailed analysis and structural characterization of proteoforms by top-down proteomics (TDP) has gained a lot of interest in biomedical research. Data-dependent acquisition (DDA) of intact proteins is non-trivial due to the diversity and complexity of proteoforms. Dedicated acquisition methods thus have the potential to greatly improve TDP. Here, we present FLASHIda, an intelligent online data acquisition algorithm for TDP that ensures the real-time selection of high-quality precursors of diverse proteoforms. FLASHIda combines fast charge deconvolution algorithms and machine learning-based quality assessment for optimal precursor selection. In an analysis of E. coli lysate, FLASHIda increases the number of unique proteoform level identifications from 800 to 1500 or generates a near-identical number of identifications in one third of the instrument time when compared to standard DDA mode. Furthermore, FLASHIda enables sensitive mapping of post-translational modifications and detection of chemical adducts. As a software extension module to the instrument, FLASHIda can be readily adopted for TDP studies of complex samples to enhance proteoform identification rates. |
format | Online Article Text |
id | pubmed-9338294 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-93382942022-07-31 FLASHIda enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts Jeong, Kyowon Babović, Maša Gorshkov, Vladimir Kim, Jihyung Jensen, Ole N. Kohlbacher, Oliver Nat Commun Article The detailed analysis and structural characterization of proteoforms by top-down proteomics (TDP) has gained a lot of interest in biomedical research. Data-dependent acquisition (DDA) of intact proteins is non-trivial due to the diversity and complexity of proteoforms. Dedicated acquisition methods thus have the potential to greatly improve TDP. Here, we present FLASHIda, an intelligent online data acquisition algorithm for TDP that ensures the real-time selection of high-quality precursors of diverse proteoforms. FLASHIda combines fast charge deconvolution algorithms and machine learning-based quality assessment for optimal precursor selection. In an analysis of E. coli lysate, FLASHIda increases the number of unique proteoform level identifications from 800 to 1500 or generates a near-identical number of identifications in one third of the instrument time when compared to standard DDA mode. Furthermore, FLASHIda enables sensitive mapping of post-translational modifications and detection of chemical adducts. As a software extension module to the instrument, FLASHIda can be readily adopted for TDP studies of complex samples to enhance proteoform identification rates. Nature Publishing Group UK 2022-07-29 /pmc/articles/PMC9338294/ /pubmed/35906205 http://dx.doi.org/10.1038/s41467-022-31922-z Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Jeong, Kyowon Babović, Maša Gorshkov, Vladimir Kim, Jihyung Jensen, Ole N. Kohlbacher, Oliver FLASHIda enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts |
title | FLASHIda enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts |
title_full | FLASHIda enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts |
title_fullStr | FLASHIda enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts |
title_full_unstemmed | FLASHIda enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts |
title_short | FLASHIda enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts |
title_sort | flashida enables intelligent data acquisition for top–down proteomics to boost proteoform identification counts |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9338294/ https://www.ncbi.nlm.nih.gov/pubmed/35906205 http://dx.doi.org/10.1038/s41467-022-31922-z |
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