Amino acids 15–28 in the ectodomain of SARS coronavirus 3a protein induces neutralizing antibodies
Identifieur interne : 000793 ( new/Analysis ); précédent : 000792; suivant : 000794Amino acids 15–28 in the ectodomain of SARS coronavirus 3a protein induces neutralizing antibodies
Auteurs : Sara Kerström [Suède] ; Yee-Joo Tan [Singapour] ; Ali Mirazimi [Suède]Source :
- Febs Letters [ 0014-5793 ] ; 2006.
Abstract
A synthetic peptide corresponding to amino acids (aa) 15–28 of the severe acute respiratory syndrome coronavirus (SARS-CoV) 3a protein was used to raise polyclonal antibodies in rabbits. This anti-3a N-terminal antibody could detect 3a protein in infected cells, as did an anti-3a C-terminal antibody previously described. The latter targeted the C-terminal cytoplasmic domain of 3a (aa 134–274). The anti-3a N-terminal antibody could detect intracellular 3a as well as 3a expressed on the cell surface. Interestingly, only the anti-3a N-terminal antibody can inhibit SARS-CoV propagation in Vero E6 culture although the binding affinity of the anti-3a N-terminal antibody was lower than the anti-3a C-terminal antibody.
Url:
DOI: 10.1016/j.febslet.2006.06.002
PubMed: 16781713
PubMed Central: 7094653
Affiliations:
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PMC:7094653Le document en format XML
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type="wicri:Area/new/Extraction">000793</idno></publicationStmt><sourceDesc><biblStruct><analytic><title xml:lang="en" level="a" type="main">Amino acids 15–28 in the ectodomain of SARS coronavirus 3a protein induces neutralizing antibodies</title><author><name sortKey=" Kerstrom, Sara" sort=" Kerstrom, Sara" uniqKey=" Kerstrom S" first="Sara" last=" Kerström">Sara Kerström</name><affiliation wicri:level="1"><nlm:aff id="aff1">Center for Microbiological Preparedness, Swedish Institute for Infectious Disease Control, SE-171 82 Solna, Sweden</nlm:aff><country xml:lang="fr">Suède</country><wicri:regionArea>Center for Microbiological Preparedness, Swedish Institute for Infectious Disease Control, SE-171 82 Solna</wicri:regionArea><wicri:noRegion>SE-171 82 Solna</wicri:noRegion></affiliation></author><author><name sortKey="Tan, Yee Joo" sort="Tan, Yee Joo" uniqKey="Tan Y" first="Yee-Joo" last="Tan">Yee-Joo Tan</name><affiliation wicri:level="1"><nlm:aff id="aff2">Institute of Molecular and Cell Biology, CAVR, 61 Biopolis Drive, Singapore 138673, Singapore</nlm:aff><country xml:lang="fr">Singapour</country><wicri:regionArea>Institute of Molecular and Cell Biology, CAVR, 61 Biopolis Drive, Singapore 138673</wicri:regionArea><wicri:noRegion>Singapore 138673</wicri:noRegion></affiliation></author><author><name sortKey="Mirazimi, Ali" sort="Mirazimi, Ali" uniqKey="Mirazimi A" first="Ali" last="Mirazimi">Ali Mirazimi</name><affiliation wicri:level="1"><nlm:aff id="aff1">Center for Microbiological Preparedness, Swedish Institute for Infectious Disease Control, SE-171 82 Solna, Sweden</nlm:aff><country xml:lang="fr">Suède</country><wicri:regionArea>Center for Microbiological Preparedness, Swedish Institute for Infectious Disease Control, SE-171 82 Solna</wicri:regionArea><wicri:noRegion>SE-171 82 Solna</wicri:noRegion></affiliation></author></analytic><series><title level="j">Febs Letters</title><idno type="ISSN">0014-5793</idno><idno type="eISSN">1873-3468</idno><imprint><date when="2006">2006</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p>A synthetic peptide corresponding to amino acids (aa) 15–28 of the severe acute respiratory syndrome coronavirus (SARS-CoV) 3a protein was used to raise polyclonal antibodies in rabbits. This anti-3a N-terminal antibody could detect 3a protein in infected cells, as did an anti-3a C-terminal antibody previously described. The latter targeted the C-terminal cytoplasmic domain of 3a (aa 134–274). The anti-3a N-terminal antibody could detect intracellular 3a as well as 3a expressed on the cell surface. Interestingly, only the anti-3a N-terminal antibody can inhibit SARS-CoV propagation in Vero E6 culture although the binding affinity of the anti-3a N-terminal antibody was lower than the anti-3a C-terminal antibody.</p></div></front><back><div1 type="bibliography"><listBibl><biblStruct><analytic><author><name sortKey="Marra, M A" uniqKey="Marra M">M.A. Marra</name></author><author><name sortKey="Jones, S J" uniqKey="Jones S">S.J. Jones</name></author><author><name sortKey="Astell, C R" uniqKey="Astell C">C.R. Astell</name></author><author><name sortKey="Holt, R A" uniqKey="Holt R">R.A. 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Kuiken</name></author></analytic></biblStruct></listBibl></div1></back></TEI><affiliations><list><country><li>Singapour</li><li>Suède</li></country></list><tree><country name="Suède"><noRegion><name sortKey=" Kerstrom, Sara" sort=" Kerstrom, Sara" uniqKey=" Kerstrom S" first="Sara" last=" Kerström">Sara Kerström</name></noRegion><name sortKey="Mirazimi, Ali" sort="Mirazimi, Ali" uniqKey="Mirazimi A" first="Ali" last="Mirazimi">Ali Mirazimi</name></country><country name="Singapour"><noRegion><name sortKey="Tan, Yee Joo" sort="Tan, Yee Joo" uniqKey="Tan Y" first="Yee-Joo" last="Tan">Yee-Joo Tan</name></noRegion></country></tree></affiliations></record>Pour manipuler ce document sous Unix (Dilib)
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