<?xml version="1.0" encoding="UTF-8"?><?xml-stylesheet type="text/xsl" href="static/style.xsl"?><OAI-PMH xmlns="http://www.openarchives.org/OAI/2.0/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/ http://www.openarchives.org/OAI/2.0/OAI-PMH.xsd"><responseDate>2026-05-22T03:09:10Z</responseDate><request verb="GetRecord" identifier="oai:repisalud.isciii.es:20.500.12105/17180" metadataPrefix="marc">https://repisalud.isciii.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:repisalud.isciii.es:20.500.12105/17180</identifier><datestamp>2025-04-25T07:37:03Z</datestamp><setSpec>com_20.500.12105_2052</setSpec><setSpec>com_20.500.12105_2051</setSpec><setSpec>col_20.500.12105_19609</setSpec></header><metadata><record xmlns="http://www.loc.gov/MARC21/slim" xmlns:dcterms="http://purl.org/dc/terms/" xmlns:doc="http://www.lyncode.com/xoai" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.loc.gov/MARC21/slim http://www.loc.gov/standards/marcxml/schema/MARC21slim.xsd">
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      <subfield code="a">Luque, Daniel</subfield>
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      <subfield code="a">Ortega-Esteban, Alvaro</subfield>
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      <subfield code="a">Valbuena, Alejandro</subfield>
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      <subfield code="a">Vilas, Jose Luis</subfield>
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      <subfield code="a">Rodríguez-Huete, Alicia</subfield>
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   <datafield ind2=" " ind1=" " tag="720">
      <subfield code="a">Mateu, Mauricio G</subfield>
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      <subfield code="a">Castón, José R</subfield>
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   <datafield ind2=" " ind1=" " tag="260">
      <subfield code="c">2023-04-15</subfield>
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      <subfield code="a">The biological function of macromolecular complexes depends not only on large-scale transitions between conformations, but also on small-scale conformational fluctuations at equilibrium. Information on the equilibrium dynamics of biomolecular complexes could, in principle, be obtained from local resolution (LR) data in cryo-electron microscopy (cryo-EM) maps. However, this possibility had not been validated by comparing, for a same biomolecular complex, LR data with quantitative information on equilibrium dynamics obtained by an established solution technique. In this study we determined the cryo-EM structure of the minute virus of mice (MVM) capsid as a model biomolecular complex. The LR values obtained correlated with crystallographic B factors and with hydrogen/deuterium exchange (HDX) rates obtained by mass spectrometry (HDX-MS), a gold standard for determining equilibrium dynamics in solution. This result validated a LR-based cryo-EM approach to investigate, with high spatial resolution, the equilibrium dynamics of biomolecular complexes. As an application of this approach, we determined the cryo-EM structure of two mutant MVM capsids and compared their equilibrium dynamics with that of the wild-type MVM capsid. The results supported a previously suggested linkage between mechanical stiffening and impaired equilibrium dynamics of a virus particle. Cryo-EM is emerging as a powerful approach for simultaneously acquiring information on the atomic structure and local equilibrium dynamics of biomolecular complexes.</subfield>
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      <subfield code="a">J Mol Biol. 2023 Apr 15;435(8):168024.</subfield>
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      <subfield code="a">10.1016/j.jmb.2023.168024</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">1089-8638</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">Journal of molecular biology</subfield>
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      <subfield code="a">36828271</subfield>
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   <datafield ind1="8" ind2=" " tag="024">
      <subfield code="a">http://hdl.handle.net/20.500.12105/17180</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Equilibrium dynamics</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Mechanical elasticity</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Cryo-electron microscopy</subfield>
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   <datafield tag="653" ind2=" " ind1=" ">
      <subfield code="a">Atomic force microscopy</subfield>
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      <subfield code="a">Virus capsid</subfield>
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   <datafield ind2="0" ind1="0" tag="245">
      <subfield code="a">Equilibrium Dynamics of a Biomolecular Complex Analyzed at Single-amino Acid Resolution by Cryo-electron Microscopy</subfield>
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