SrasV1, PubMed, Checkpoint, bibRecord, 001660

Identification of NCAM that interacts with the PHE-CoV spike protein.

Identifieur interne : 001660 ( PubMed/Checkpoint ); précédent : 001659; suivant : 001661

Identification of NCAM that interacts with the PHE-CoV spike protein.

Auteurs : Wei Gao [République populaire de Chine] ; Wenqi He ; Kui Zhao ; Huijun Lu ; Wenzhi Ren ; Chongtao Du ; Keyan Chen ; Yungang Lan ; Deguang Song ; Feng Gao

Source :

Virology journal [ 1743-422X ] ; 2010.

RBID : pubmed:20863409

Descripteurs français

English descriptors

KwdEn :
- Animals, Cell Line, Coronavirus (pathogenicity), Gene Silencing, Host-Pathogen Interactions, Immunoprecipitation, Membrane Glycoproteins (metabolism), Mice, Neural Cell Adhesion Molecules (metabolism), Peptide Library, Podoviridae (genetics), Protein Binding, RNA, Small Interfering (genetics), RNA, Small Interfering (metabolism), Spike Glycoprotein, Coronavirus, Viral Envelope Proteins (metabolism).
MESH :
- chemical , genetics : RNA, Small Interfering.
- chemical , metabolism : Membrane Glycoproteins, Neural Cell Adhesion Molecules, RNA, Small Interfering, Viral Envelope Proteins.
- genetics : Podoviridae.
- pathogenicity : Coronavirus.
- Animals, Cell Line, Gene Silencing, Host-Pathogen Interactions, Immunoprecipitation, Mice, Peptide Library, Protein Binding, Spike Glycoprotein, Coronavirus.

Abstract

The spike proteins of coronaviruses associate with cellular molecules to mediate infection of their target cells. The characterization of cellular proteins required for virus infection is essential for understanding viral life cycles and may provide cellular targets for antiviral therapies.

DOI: 10.1186/1743-422X-7-254
PubMed: 20863409

Affiliations:

Links toward previous steps (curation, corpus...)

to stream PubMed, to step Corpus: 001625
to stream PubMed, to step Curation: 001625

Links to Exploration step

pubmed:20863409

Le document en format XML

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<author><name sortKey="Lan, Yungang" sort="Lan, Yungang" uniqKey="Lan Y" first="Yungang" last="Lan">Yungang Lan</name>
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<author><name sortKey="Song, Deguang" sort="Song, Deguang" uniqKey="Song D" first="Deguang" last="Song">Deguang Song</name>
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<author><name sortKey="Song, Deguang" sort="Song, Deguang" uniqKey="Song D" first="Deguang" last="Song">Deguang Song</name>
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<term>Cell Line</term>
<term>Coronavirus (pathogenicity)</term>
<term>Gene Silencing</term>
<term>Host-Pathogen Interactions</term>
<term>Immunoprecipitation</term>
<term>Membrane Glycoproteins (metabolism)</term>
<term>Mice</term>
<term>Neural Cell Adhesion Molecules (metabolism)</term>
<term>Peptide Library</term>
<term>Podoviridae (genetics)</term>
<term>Protein Binding</term>
<term>RNA, Small Interfering (genetics)</term>
<term>RNA, Small Interfering (metabolism)</term>
<term>Spike Glycoprotein, Coronavirus</term>
<term>Viral Envelope Proteins (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr"><term>Animaux</term>
<term>Banque de peptides</term>
<term>Coronavirus (pathogénicité)</term>
<term>Extinction de l'expression des gènes</term>
<term>Glycoprotéine de spicule des coronavirus</term>
<term>Glycoprotéines membranaires (métabolisme)</term>
<term>Immunoprécipitation</term>
<term>Interactions hôte-pathogène</term>
<term>Liaison aux protéines</term>
<term>Lignée cellulaire</term>
<term>Molécules d'adhérence cellulaire neurales (métabolisme)</term>
<term>Petit ARN interférent (génétique)</term>
<term>Petit ARN interférent (métabolisme)</term>
<term>Podoviridae (génétique)</term>
<term>Protéines de l'enveloppe virale (métabolisme)</term>
<term>Souris</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>RNA, Small Interfering</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en"><term>Membrane Glycoproteins</term>
<term>Neural Cell Adhesion Molecules</term>
<term>RNA, Small Interfering</term>
<term>Viral Envelope Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en"><term>Podoviridae</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr"><term>Petit ARN interférent</term>
<term>Podoviridae</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr"><term>Glycoprotéines membranaires</term>
<term>Molécules d'adhérence cellulaire neurales</term>
<term>Petit ARN interférent</term>
<term>Protéines de l'enveloppe virale</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogenicity" xml:lang="en"><term>Coronavirus</term>
</keywords>
<keywords scheme="MESH" qualifier="pathogénicité" xml:lang="fr"><term>Coronavirus</term>
</keywords>
<keywords scheme="MESH" xml:lang="en"><term>Animals</term>
<term>Cell Line</term>
<term>Gene Silencing</term>
<term>Host-Pathogen Interactions</term>
<term>Immunoprecipitation</term>
<term>Mice</term>
<term>Peptide Library</term>
<term>Protein Binding</term>
<term>Spike Glycoprotein, Coronavirus</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr"><term>Animaux</term>
<term>Banque de peptides</term>
<term>Extinction de l'expression des gènes</term>
<term>Glycoprotéine de spicule des coronavirus</term>
<term>Immunoprécipitation</term>
<term>Interactions hôte-pathogène</term>
<term>Liaison aux protéines</term>
<term>Lignée cellulaire</term>
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<front><div type="abstract" xml:lang="en">The spike proteins of coronaviruses associate with cellular molecules to mediate infection of their target cells. The characterization of cellular proteins required for virus infection is essential for understanding viral life cycles and may provide cellular targets for antiviral therapies.</div>
</front>
</TEI>
<pubmed><MedlineCitation Status="MEDLINE" Owner="NLM"><PMID Version="1">20863409</PMID>
<DateCompleted><Year>2010</Year>
<Month>12</Month>
<Day>01</Day>
</DateCompleted>
<DateRevised><Year>2020</Year>
<Month>04</Month>
<Day>15</Day>
</DateRevised>
<Article PubModel="Electronic"><Journal><ISSN IssnType="Electronic">1743-422X</ISSN>
<JournalIssue CitedMedium="Internet"><Volume>7</Volume>
<PubDate><Year>2010</Year>
<Month>Sep</Month>
<Day>24</Day>
</PubDate>
</JournalIssue>
<Title>Virology journal</Title>
<ISOAbbreviation>Virol. J.</ISOAbbreviation>
</Journal>
<ArticleTitle>Identification of NCAM that interacts with the PHE-CoV spike protein.</ArticleTitle>
<Pagination><MedlinePgn>254</MedlinePgn>
</Pagination>
<ELocationID EIdType="doi" ValidYN="Y">10.1186/1743-422X-7-254</ELocationID>
<Abstract><AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">The spike proteins of coronaviruses associate with cellular molecules to mediate infection of their target cells. The characterization of cellular proteins required for virus infection is essential for understanding viral life cycles and may provide cellular targets for antiviral therapies.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">We identified Neural Cell Adhesion Molecule (NCAM) as a novel interacting partner of the PHE-CoV S protein. A T7 phage display cDNA library from N2a cells was constructed, and the library was screened with the soluble PHE-CoV S glycoproteins. We used a coimmunoprecipitation assay to show that only the NCAM was a binding partner of spike protein. We found that a soluble form of anti-NCAM antibody blocked association of the PHE-CoV with N2a cells. Furthermore, double-stranded siRNA targeted against NCAM inhibited PHE-CoV infection.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">A novel interaction was identified between NCAM and spike protein and this association is critical during PHE-CoV infection.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y"><Author ValidYN="Y"><LastName>Gao</LastName>
<ForeName>Wei</ForeName>
<Initials>W</Initials>
<AffiliationInfo><Affiliation>College of Animal Science and Veterinary Medicine, Jilin University, Changchun, PR China.</Affiliation>
</AffiliationInfo>
</Author>
<Author ValidYN="Y"><LastName>He</LastName>
<ForeName>Wenqi</ForeName>
<Initials>W</Initials>
</Author>
<Author ValidYN="Y"><LastName>Zhao</LastName>
<ForeName>Kui</ForeName>
<Initials>K</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lu</LastName>
<ForeName>Huijun</ForeName>
<Initials>H</Initials>
</Author>
<Author ValidYN="Y"><LastName>Ren</LastName>
<ForeName>Wenzhi</ForeName>
<Initials>W</Initials>
</Author>
<Author ValidYN="Y"><LastName>Du</LastName>
<ForeName>Chongtao</ForeName>
<Initials>C</Initials>
</Author>
<Author ValidYN="Y"><LastName>Chen</LastName>
<ForeName>Keyan</ForeName>
<Initials>K</Initials>
</Author>
<Author ValidYN="Y"><LastName>Lan</LastName>
<ForeName>Yungang</ForeName>
<Initials>Y</Initials>
</Author>
<Author ValidYN="Y"><LastName>Song</LastName>
<ForeName>Deguang</ForeName>
<Initials>D</Initials>
</Author>
<Author ValidYN="Y"><LastName>Gao</LastName>
<ForeName>Feng</ForeName>
<Initials>F</Initials>
</Author>
</AuthorList>
<Language>eng</Language>
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<PublicationType UI="D013485">Research Support, Non-U.S. Gov't</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic"><Year>2010</Year>
<Month>09</Month>
<Day>24</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo><Country>England</Country>
<MedlineTA>Virol J</MedlineTA>
<NlmUniqueID>101231645</NlmUniqueID>
<ISSNLinking>1743-422X</ISSNLinking>
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<ChemicalList><Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C578553">MHV surface projection glycoprotein</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D008562">Membrane Glycoproteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D019006">Neural Cell Adhesion Molecules</NameOfSubstance>
</Chemical>
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<NameOfSubstance UI="D064370">Spike Glycoprotein, Coronavirus</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="D014759">Viral Envelope Proteins</NameOfSubstance>
</Chemical>
<Chemical><RegistryNumber>0</RegistryNumber>
<NameOfSubstance UI="C578557">spike glycoprotein, SARS-CoV</NameOfSubstance>
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<MeshHeading><DescriptorName UI="D019006" MajorTopicYN="N">Neural Cell Adhesion Molecules</DescriptorName>
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</MeshHeading>
<MeshHeading><DescriptorName UI="D019151" MajorTopicYN="N">Peptide Library</DescriptorName>
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<QualifierName UI="Q000235" MajorTopicYN="N">genetics</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D011485" MajorTopicYN="N">Protein Binding</DescriptorName>
</MeshHeading>
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<QualifierName UI="Q000378" MajorTopicYN="N">metabolism</QualifierName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D064370" MajorTopicYN="N">Spike Glycoprotein, Coronavirus</DescriptorName>
</MeshHeading>
<MeshHeading><DescriptorName UI="D014759" MajorTopicYN="N">Viral Envelope Proteins</DescriptorName>
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Identification of NCAM that interacts with the PHE-CoV spike protein.

Identification of NCAM that interacts with the PHE-CoV spike protein.

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