<?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>2026-05-30T10:20:27Z</responseDate><request verb="GetRecord" identifier="oai:riuma.uma.es:10630/38172" metadataPrefix="marc">https://riuma.uma.es/rest/oai/request</request><GetRecord><record><header><identifier>oai:riuma.uma.es:10630/38172</identifier><datestamp>2026-02-03T11:17:16Z</datestamp><setSpec>com_10630_2254</setSpec><setSpec>col_10630_37953</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">Burnap, Sean A.</subfield>
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      <subfield code="a">Ortega-Prieto, Ana María</subfield>
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      <subfield code="a">Jimenez-Guardeño, Jose Manuel</subfield>
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      <subfield code="a">Ali, Hashim</subfield>
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      <subfield code="a">Takov, Kaloyan</subfield>
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      <subfield code="a">Fish, Matthew</subfield>
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      <subfield code="a">Shankar-Hari, Manu</subfield>
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      <subfield code="a">Giacca, Mauro</subfield>
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      <subfield code="a">Malim, Michael H.</subfield>
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      <subfield code="a">Mayr, Manuel</subfield>
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      <subfield code="c">2023</subfield>
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      <subfield code="a">High-density lipoprotein (HDL) levels are reduced in patients with coronavirus disease 2019 (COVID-19), and the extent of this reduction is associated with poor clinical outcomes. While lipoproteins are known to play a key role during the life cycle of the hepatitis C virus, their influence on coronavirus (CoV) infections is poorly understood. In this study, we utilize cross-linking mass spectrometry (XL-MS) to determine circulating protein interactors of the severe acute respiratory syndrome (SARS)-CoV-2 spike glycoprotein. XL-MS of plasma isolated from patients with COVID-19 uncovered HDL protein interaction networks, dominated by acute-phase serum amyloid proteins, whereby serum amyloid A2 was shown to bind to apolipoprotein (Apo) D. XL-MS on isolated HDL confirmed ApoD to interact with SARS-CoV-2 spike but not SARS-CoV-1 spike. Other direct interactions of SARS-CoV-2 spike upon HDL included ApoA1 and ApoC3. The interaction between ApoD and spike was further validated in cells using immunoprecipitation-MS, which uncovered a novel interaction between both ApoD and spike with membrane-associated progesterone receptor component 1. Mechanistically, XL-MS coupled with data-driven structural modeling determined that ApoD may interact within the receptor-binding domain of the spike. However, ApoD overexpression in multiple cell-based assays had no effect upon viral replication or infectivity. Thus, SARS-CoV-2 spike can bind to apolipoproteins on HDL, but these interactions do not appear to alter infectivity.</subfield>
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      <subfield code="a">https://hdl.handle.net/10630/38172</subfield>
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      <subfield code="a">10.1016/j.mcpro.2023.100600</subfield>
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      <subfield code="a">COVID-19 - Aspectos moleculares</subfield>
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      <subfield code="a">Virología</subfield>
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      <subfield code="a">Cross-Linking Mass Spectrometry Uncovers Interactions Between High-Density Lipoproteins and the SARS-CoV-2 Spike Glycoprotein.</subfield>
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