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HDX-MS: An Analytical Tool to Capture Protein Motion in Action

Virtually all protein functions in the cell, including pathogenic processes, require coordinated motion of atoms or domains, i.e., conformational dynamics. Understanding protein dynamics is therefore critical both for drug development and to learn about the underlying molecular causes of many diseas...

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Detalles Bibliográficos
Autores principales: Narang, Dominic, Lento, Cristina, J. Wilson, Derek
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399943/
https://www.ncbi.nlm.nih.gov/pubmed/32709043
http://dx.doi.org/10.3390/biomedicines8070224
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author Narang, Dominic
Lento, Cristina
J. Wilson, Derek
author_facet Narang, Dominic
Lento, Cristina
J. Wilson, Derek
author_sort Narang, Dominic
collection PubMed
description Virtually all protein functions in the cell, including pathogenic processes, require coordinated motion of atoms or domains, i.e., conformational dynamics. Understanding protein dynamics is therefore critical both for drug development and to learn about the underlying molecular causes of many diseases. Hydrogen–Deuterium Exchange Mass Spectrometry (HDX-MS) provides valuable information about protein dynamics, which is highly complementary to the static picture provided by conventional high-resolution structural tools (i.e., X-ray crystallography and structural NMR). The amount of protein required to carry out HDX-MS experiments is a fraction of the amount required by alternative biophysical techniques, which are also usually lower resolution. Use of HDX-MS is growing quickly both in industry and academia, and it has been successfully used in numerous drug and vaccine development efforts, with important roles in understanding allosteric effects and mapping binding sites.
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spelling pubmed-73999432020-08-17 HDX-MS: An Analytical Tool to Capture Protein Motion in Action Narang, Dominic Lento, Cristina J. Wilson, Derek Biomedicines Review Virtually all protein functions in the cell, including pathogenic processes, require coordinated motion of atoms or domains, i.e., conformational dynamics. Understanding protein dynamics is therefore critical both for drug development and to learn about the underlying molecular causes of many diseases. Hydrogen–Deuterium Exchange Mass Spectrometry (HDX-MS) provides valuable information about protein dynamics, which is highly complementary to the static picture provided by conventional high-resolution structural tools (i.e., X-ray crystallography and structural NMR). The amount of protein required to carry out HDX-MS experiments is a fraction of the amount required by alternative biophysical techniques, which are also usually lower resolution. Use of HDX-MS is growing quickly both in industry and academia, and it has been successfully used in numerous drug and vaccine development efforts, with important roles in understanding allosteric effects and mapping binding sites. MDPI 2020-07-17 /pmc/articles/PMC7399943/ /pubmed/32709043 http://dx.doi.org/10.3390/biomedicines8070224 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Narang, Dominic
Lento, Cristina
J. Wilson, Derek
HDX-MS: An Analytical Tool to Capture Protein Motion in Action
title HDX-MS: An Analytical Tool to Capture Protein Motion in Action
title_full HDX-MS: An Analytical Tool to Capture Protein Motion in Action
title_fullStr HDX-MS: An Analytical Tool to Capture Protein Motion in Action
title_full_unstemmed HDX-MS: An Analytical Tool to Capture Protein Motion in Action
title_short HDX-MS: An Analytical Tool to Capture Protein Motion in Action
title_sort hdx-ms: an analytical tool to capture protein motion in action
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7399943/
https://www.ncbi.nlm.nih.gov/pubmed/32709043
http://dx.doi.org/10.3390/biomedicines8070224
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