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Advances in Hydrogen/Deuterium Exchange Mass Spectrometry and the Pursuit of Challenging Biological Systems
[Image: see text] Solution-phase hydrogen/deuterium exchange (HDX) coupled to mass spectrometry (MS) is a widespread tool for structural analysis across academia and the biopharmaceutical industry. By monitoring the exchangeability of backbone amide protons, HDX-MS can reveal information about highe...
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/PMC9053315/ https://www.ncbi.nlm.nih.gov/pubmed/34493042 http://dx.doi.org/10.1021/acs.chemrev.1c00279 |
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author | James, Ellie I. Murphree, Taylor A. Vorauer, Clint Engen, John R. Guttman, Miklos |
author_facet | James, Ellie I. Murphree, Taylor A. Vorauer, Clint Engen, John R. Guttman, Miklos |
author_sort | James, Ellie I. |
collection | PubMed |
description | [Image: see text] Solution-phase hydrogen/deuterium exchange (HDX) coupled to mass spectrometry (MS) is a widespread tool for structural analysis across academia and the biopharmaceutical industry. By monitoring the exchangeability of backbone amide protons, HDX-MS can reveal information about higher-order structure and dynamics throughout a protein, can track protein folding pathways, map interaction sites, and assess conformational states of protein samples. The combination of the versatility of the hydrogen/deuterium exchange reaction with the sensitivity of mass spectrometry has enabled the study of extremely challenging protein systems, some of which cannot be suitably studied using other techniques. Improvements over the past three decades have continually increased throughput, robustness, and expanded the limits of what is feasible for HDX-MS investigations. To provide an overview for researchers seeking to utilize and derive the most from HDX-MS for protein structural analysis, we summarize the fundamental principles, basic methodology, strengths and weaknesses, and the established applications of HDX-MS while highlighting new developments and applications. |
format | Online Article Text |
id | pubmed-9053315 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-90533152022-09-07 Advances in Hydrogen/Deuterium Exchange Mass Spectrometry and the Pursuit of Challenging Biological Systems James, Ellie I. Murphree, Taylor A. Vorauer, Clint Engen, John R. Guttman, Miklos Chem Rev [Image: see text] Solution-phase hydrogen/deuterium exchange (HDX) coupled to mass spectrometry (MS) is a widespread tool for structural analysis across academia and the biopharmaceutical industry. By monitoring the exchangeability of backbone amide protons, HDX-MS can reveal information about higher-order structure and dynamics throughout a protein, can track protein folding pathways, map interaction sites, and assess conformational states of protein samples. The combination of the versatility of the hydrogen/deuterium exchange reaction with the sensitivity of mass spectrometry has enabled the study of extremely challenging protein systems, some of which cannot be suitably studied using other techniques. Improvements over the past three decades have continually increased throughput, robustness, and expanded the limits of what is feasible for HDX-MS investigations. To provide an overview for researchers seeking to utilize and derive the most from HDX-MS for protein structural analysis, we summarize the fundamental principles, basic methodology, strengths and weaknesses, and the established applications of HDX-MS while highlighting new developments and applications. American Chemical Society 2021-09-07 2022-04-27 /pmc/articles/PMC9053315/ /pubmed/34493042 http://dx.doi.org/10.1021/acs.chemrev.1c00279 Text en © 2021 The Authors. Published by American Chemical Society https://creativecommons.org/licenses/by-nc-nd/4.0/Permits non-commercial access and re-use, provided that author attribution and integrity are maintained; but does not permit creation of adaptations or other derivative works (https://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | James, Ellie I. Murphree, Taylor A. Vorauer, Clint Engen, John R. Guttman, Miklos Advances in Hydrogen/Deuterium Exchange Mass Spectrometry and the Pursuit of Challenging Biological Systems |
title | Advances in Hydrogen/Deuterium Exchange Mass Spectrometry
and the Pursuit of Challenging Biological Systems |
title_full | Advances in Hydrogen/Deuterium Exchange Mass Spectrometry
and the Pursuit of Challenging Biological Systems |
title_fullStr | Advances in Hydrogen/Deuterium Exchange Mass Spectrometry
and the Pursuit of Challenging Biological Systems |
title_full_unstemmed | Advances in Hydrogen/Deuterium Exchange Mass Spectrometry
and the Pursuit of Challenging Biological Systems |
title_short | Advances in Hydrogen/Deuterium Exchange Mass Spectrometry
and the Pursuit of Challenging Biological Systems |
title_sort | advances in hydrogen/deuterium exchange mass spectrometry
and the pursuit of challenging biological systems |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9053315/ https://www.ncbi.nlm.nih.gov/pubmed/34493042 http://dx.doi.org/10.1021/acs.chemrev.1c00279 |
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