Severe acute respiratory syndrome coronavirus accessory proteins 6 and 9b interact in vivo.
Identifieur interne : 001C55 ( Main/Exploration ); précédent : 001C54; suivant : 001C56Severe acute respiratory syndrome coronavirus accessory proteins 6 and 9b interact in vivo.
Auteurs : Enrique Calvo [Espagne] ; Marta L. Dediego ; Pilar García ; Juan A. L Pez ; Pilar Pérez-Bre A ; Ana Falc NSource :
- Virus research [ 1872-7492 ] ; 2012.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , metabolism : Viral Regulatory and Accessory Proteins.
- physiology : SARS Virus.
- Amino Acid Sequence, Animals, Chlorocebus aethiops, Immunoprecipitation, Mass Spectrometry, Molecular Sequence Data, Protein Interaction Mapping, Vero Cells.
Abstract
The 3'proximal one-third of the severe acute respiratory syndrome coronavirus (SARS-CoV) genome encodes the structural proteins and eight accessory proteins, including 3a, 3b, 6, 7a, 7b, 8a, 8b and 9b, varying in length from 39 to 274aa which do not share significant homology with viral proteins of known coronaviruses. The SARS-CoV protein 6 is 63 amino acids in length and has been previously involved in virus pathogenicity and replication. To further analyze this functions, the interaction of SARS-CoV protein 6 with other viral and/or cellular factors has been analyzed during SARS-CoV infective cycle. Protein 6 immunoprecipitation from extracts of SARS-CoV infected cells and mass spectrometry analysis revealed an interaction of viral proteins 6 and 9b in biologically relevant conditions. This interaction has been reinforced by co-localization of both proteins in the cytoplasm of SARS-CoV infected cells.
DOI: 10.1016/j.virusres.2012.07.012
PubMed: 22820404
Affiliations:
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Le document en format XML
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<term>Molecular Sequence Data</term>
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<term>Viral Regulatory and Accessory Proteins (metabolism)</term>
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<term>Immunoprécipitation</term>
<term>Protéines virales régulatrices ou accessoires (métabolisme)</term>
<term>Spectrométrie de masse</term>
<term>Séquence d'acides aminés</term>
<term>Virus du SRAS (physiologie)</term>
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<term>Mass Spectrometry</term>
<term>Molecular Sequence Data</term>
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<term>Cartographie d'interactions entre protéines</term>
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<front><div type="abstract" xml:lang="en">The 3'proximal one-third of the severe acute respiratory syndrome coronavirus (SARS-CoV) genome encodes the structural proteins and eight accessory proteins, including 3a, 3b, 6, 7a, 7b, 8a, 8b and 9b, varying in length from 39 to 274aa which do not share significant homology with viral proteins of known coronaviruses. The SARS-CoV protein 6 is 63 amino acids in length and has been previously involved in virus pathogenicity and replication. To further analyze this functions, the interaction of SARS-CoV protein 6 with other viral and/or cellular factors has been analyzed during SARS-CoV infective cycle. Protein 6 immunoprecipitation from extracts of SARS-CoV infected cells and mass spectrometry analysis revealed an interaction of viral proteins 6 and 9b in biologically relevant conditions. This interaction has been reinforced by co-localization of both proteins in the cytoplasm of SARS-CoV infected cells.</div>
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<country name="Espagne"><region name="Communauté de Madrid"><name sortKey="Calvo, Enrique" sort="Calvo, Enrique" uniqKey="Calvo E" first="Enrique" last="Calvo">Enrique Calvo</name>
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