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Structural dynamics: review of time-resolved cryo-EM

The structural determination of biological macromolecules has been transformative for understanding biochemical mechanisms and developing therapeutics. However, the ultimate goal of characterizing how structural dynamics underpin biochemical processes has been difficult. This is largely due to signi...

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Detalles Bibliográficos
Autores principales: Mäeots, Märt-Erik, Enchev, Radoslav I.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Union of Crystallography 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344476/
https://www.ncbi.nlm.nih.gov/pubmed/35916218
http://dx.doi.org/10.1107/S2059798322006155
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author Mäeots, Märt-Erik
Enchev, Radoslav I.
author_facet Mäeots, Märt-Erik
Enchev, Radoslav I.
author_sort Mäeots, Märt-Erik
collection PubMed
description The structural determination of biological macromolecules has been transformative for understanding biochemical mechanisms and developing therapeutics. However, the ultimate goal of characterizing how structural dynamics underpin biochemical processes has been difficult. This is largely due to significant technical challenges that hinder data collection and analysis on the native timescales of macromolecular dynamics. Single-particle cryo-EM provides a powerful platform to approach this challenge, since samples can be frozen faster than the single-turnover timescales of most biochemical reactions. In order to enable time-resolved analysis, significant innovations in the handling and preparation of cryo-EM samples have been implemented, bringing us closer to the goal of the direct observation of protein dynamics in the milliseconds to seconds range. Here, the current state of time-resolved cryo-EM is reviewed and the most promising future research directions are discussed.
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spelling pubmed-93444762022-08-15 Structural dynamics: review of time-resolved cryo-EM Mäeots, Märt-Erik Enchev, Radoslav I. Acta Crystallogr D Struct Biol Ccp-EM The structural determination of biological macromolecules has been transformative for understanding biochemical mechanisms and developing therapeutics. However, the ultimate goal of characterizing how structural dynamics underpin biochemical processes has been difficult. This is largely due to significant technical challenges that hinder data collection and analysis on the native timescales of macromolecular dynamics. Single-particle cryo-EM provides a powerful platform to approach this challenge, since samples can be frozen faster than the single-turnover timescales of most biochemical reactions. In order to enable time-resolved analysis, significant innovations in the handling and preparation of cryo-EM samples have been implemented, bringing us closer to the goal of the direct observation of protein dynamics in the milliseconds to seconds range. Here, the current state of time-resolved cryo-EM is reviewed and the most promising future research directions are discussed. International Union of Crystallography 2022-07-21 /pmc/articles/PMC9344476/ /pubmed/35916218 http://dx.doi.org/10.1107/S2059798322006155 Text en © Mäeots and Enchev 2022 https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original authors and source are cited.
spellingShingle Ccp-EM
Mäeots, Märt-Erik
Enchev, Radoslav I.
Structural dynamics: review of time-resolved cryo-EM
title Structural dynamics: review of time-resolved cryo-EM
title_full Structural dynamics: review of time-resolved cryo-EM
title_fullStr Structural dynamics: review of time-resolved cryo-EM
title_full_unstemmed Structural dynamics: review of time-resolved cryo-EM
title_short Structural dynamics: review of time-resolved cryo-EM
title_sort structural dynamics: review of time-resolved cryo-em
topic Ccp-EM
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9344476/
https://www.ncbi.nlm.nih.gov/pubmed/35916218
http://dx.doi.org/10.1107/S2059798322006155
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