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Characterization of the 3a Protein of SARS-associated Coronavirus in Infected Vero E6 Cells and SARS Patients☆

Identifieur interne : 005426 ( Main/Exploration ); précédent : 005425; suivant : 005427

Characterization of the 3a Protein of SARS-associated Coronavirus in Infected Vero E6 Cells and SARS Patients☆

Auteurs : Rong Zeng [République populaire de Chine] ; Rui-Fu Yang [République populaire de Chine] ; Mu-De Shi [République populaire de Chine] ; Man-Rong Jiang [République populaire de Chine] ; You-Hua Xie [République populaire de Chine] ; Hong-Qiang Ruan [République populaire de Chine] ; Xiao-Sheng Jiang [République populaire de Chine] ; Lv Shi [République populaire de Chine] ; Hu Zhou [République populaire de Chine] ; Lei Zhang [République populaire de Chine] ; Xiao-Dong Wu [République populaire de Chine] ; Ying Lin [République populaire de Chine] ; Yong-Yong Ji [République populaire de Chine] ; Lei Xiong [République populaire de Chine] ; Yan Jin [République populaire de Chine] ; Er-Hei Dai [République populaire de Chine] ; Xiao-Yi Wang [République populaire de Chine] ; Bin-Ying Si [République populaire de Chine] ; Jin Wang [République populaire de Chine] ; Hong-Xia Wang [République populaire de Chine] ; Cui-E Wang [République populaire de Chine] ; Yong-Hua Gan [République populaire de Chine] ; Yu-Chuan Li [République populaire de Chine] ; Ju-Tian Cao [République populaire de Chine] ; Jiang-Ping Zuo [République populaire de Chine] ; Shi-Fang Shan [République populaire de Chine] ; En Xie [République populaire de Chine] ; Song-Hua Chen [République populaire de Chine] ; Zhi-Qin Jiang [République populaire de Chine] ; Xi Zhang [République populaire de Chine] ; Yuan Wang [République populaire de Chine] ; Gang Pei [République populaire de Chine] ; Bing Sun [République populaire de Chine] ; Jia-Rui Wu [République populaire de Chine]

Source :

RBID : PMC:7127270

Descripteurs français

English descriptors

Abstract

Proteomics was used to identify a protein encoded by ORF 3a in a SARS-associated coronavirus (SARS-CoV). Immuno-blotting revealed that interchain disulfide bonds might be formed between this protein and the spike protein. ELISA indicated that sera from SARS patients have significant positive reactions with synthesized peptides derived from the 3a protein. These results are concordant with that of a spike protein-derived peptide. A tendency exists for co-mutation between the 3a protein and the spike protein of SARS-CoV isolates, suggesting that the function of the 3a protein correlates with the spike protein. Taken together, the 3a protein might be tightly correlated to the spike protein in the SARS-CoV functions. The 3a protein may serve as a new clinical marker or drug target for SARS treatment.


Url:
DOI: 10.1016/j.jmb.2004.06.016
PubMed: 15312778
PubMed Central: 7127270


Affiliations:


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<nlm:aff id="AFF2">Laboratory of Molecular Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue-Yang Road, Shanghai 200031, China</nlm:aff>
<country xml:lang="fr">République populaire de Chine</country>
<wicri:regionArea>Laboratory of Molecular Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue-Yang Road, Shanghai 200031</wicri:regionArea>
<wicri:noRegion>Shanghai 200031</wicri:noRegion>
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</author>
</analytic>
<series>
<title level="j">Journal of Molecular Biology</title>
<idno type="ISSN">0022-2836</idno>
<idno type="eISSN">1089-8638</idno>
<imprint>
<date when="2004">2004</date>
</imprint>
</series>
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</fileDesc>
<profileDesc>
<textClass>
<keywords scheme="KwdEn" xml:lang="en">
<term>Animals</term>
<term>Chlorocebus aethiops</term>
<term>Disulfides (metabolism)</term>
<term>Humans</term>
<term>Membrane Glycoproteins (metabolism)</term>
<term>Phylogeny</term>
<term>Proteomics</term>
<term>SARS Virus (chemistry)</term>
<term>SARS Virus (genetics)</term>
<term>SARS Virus (metabolism)</term>
<term>Sequence Analysis, Protein</term>
<term>Spike Glycoprotein, Coronavirus</term>
<term>Vero Cells</term>
<term>Viral Envelope Proteins (metabolism)</term>
<term>Viral Proteins (chemistry)</term>
<term>Viral Proteins (genetics)</term>
<term>Viral Proteins (metabolism)</term>
</keywords>
<keywords scheme="KwdFr" xml:lang="fr">
<term>Analyse de séquence de protéine</term>
<term>Animaux</term>
<term>Cellules Vero</term>
<term>Disulfures (métabolisme)</term>
<term>Glycoprotéine de spicule des coronavirus</term>
<term>Glycoprotéines membranaires (métabolisme)</term>
<term>Humains</term>
<term>Phylogénie</term>
<term>Protéines de l'enveloppe virale (métabolisme)</term>
<term>Protéines virales ()</term>
<term>Protéines virales (génétique)</term>
<term>Protéines virales (métabolisme)</term>
<term>Protéomique</term>
<term>Virus du SRAS ()</term>
<term>Virus du SRAS (génétique)</term>
<term>Virus du SRAS (métabolisme)</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="chemistry" xml:lang="en">
<term>Viral Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en">
<term>Viral Proteins</term>
</keywords>
<keywords scheme="MESH" type="chemical" qualifier="metabolism" xml:lang="en">
<term>Disulfides</term>
<term>Membrane Glycoproteins</term>
<term>Viral Envelope Proteins</term>
<term>Viral Proteins</term>
</keywords>
<keywords scheme="MESH" qualifier="chemistry" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="genetics" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="génétique" xml:lang="fr">
<term>Protéines virales</term>
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" qualifier="metabolism" xml:lang="en">
<term>SARS Virus</term>
</keywords>
<keywords scheme="MESH" qualifier="métabolisme" xml:lang="fr">
<term>Disulfures</term>
<term>Glycoprotéines membranaires</term>
<term>Protéines de l'enveloppe virale</term>
<term>Protéines virales</term>
<term>Virus du SRAS</term>
</keywords>
<keywords scheme="MESH" xml:lang="en">
<term>Animals</term>
<term>Chlorocebus aethiops</term>
<term>Humans</term>
<term>Phylogeny</term>
<term>Proteomics</term>
<term>Sequence Analysis, Protein</term>
<term>Spike Glycoprotein, Coronavirus</term>
<term>Vero Cells</term>
</keywords>
<keywords scheme="MESH" xml:lang="fr">
<term>Analyse de séquence de protéine</term>
<term>Animaux</term>
<term>Cellules Vero</term>
<term>Glycoprotéine de spicule des coronavirus</term>
<term>Humains</term>
<term>Phylogénie</term>
<term>Protéines virales</term>
<term>Protéomique</term>
<term>Virus du SRAS</term>
</keywords>
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</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>Proteomics was used to identify a protein encoded by ORF 3a in a SARS-associated coronavirus (SARS-CoV). Immuno-blotting revealed that interchain disulfide bonds might be formed between this protein and the spike protein. ELISA indicated that sera from SARS patients have significant positive reactions with synthesized peptides derived from the 3a protein. These results are concordant with that of a spike protein-derived peptide. A tendency exists for co-mutation between the 3a protein and the spike protein of SARS-CoV isolates, suggesting that the function of the 3a protein correlates with the spike protein. Taken together, the 3a protein might be tightly correlated to the spike protein in the SARS-CoV functions. The 3a protein may serve as a new clinical marker or drug target for SARS treatment.</p>
</div>
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<li>République populaire de Chine</li>
</country>
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<li>Pékin</li>
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</country>
</tree>
</affiliations>
</record>

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