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Identification of two antigenic epitopes on SARS-CoV spike protein

The spike (S) protein of severe acute respiratory syndrome-coronavirus (SARS-CoV) is a major virion structural protein. It plays an important role in interaction with receptor and inducing neutralizing antibodies. In the study, six tentative antigenic epitopes (S1 S2 S3 S4 S5 S6) of the spike protei...

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Autores principales: Hua, Ronghong, Zhou, Yanjun, Wang, Yunfeng, Hua, Yuzhuo, Tong, Guangzhi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier Inc. 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111154/
https://www.ncbi.nlm.nih.gov/pubmed/15184071
http://dx.doi.org/10.1016/j.bbrc.2004.05.066
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author Hua, Ronghong
Zhou, Yanjun
Wang, Yunfeng
Hua, Yuzhuo
Tong, Guangzhi
author_facet Hua, Ronghong
Zhou, Yanjun
Wang, Yunfeng
Hua, Yuzhuo
Tong, Guangzhi
author_sort Hua, Ronghong
collection PubMed
description The spike (S) protein of severe acute respiratory syndrome-coronavirus (SARS-CoV) is a major virion structural protein. It plays an important role in interaction with receptor and inducing neutralizing antibodies. In the study, six tentative antigenic epitopes (S1 S2 S3 S4 S5 S6) of the spike protein of SARS-CoV were predicted by bio-informatics analysis, and a multi-epitope chimeric gene of S1–S2–S3–S4–S5–S6 was synthesized and fused to downstream GST gene in pGEX-6p-1. The Western blotting demonstrated that SARS patient convalescent serum could recognize the recombinant fusion protein. A number of monoclonal antibodies were developed against the fusion protein. In further, the six predicted epitope genes were individually fused to GST of pGEX-6p-1 and expressed in Escherichia coli BL21, respectively. Among six fusion peptides, S5 reacted with monoclonal antibody D3C5 and S2 reacted with monoclonal antibody D3D1 against spike protein of SARS-CoV. The epitopes recognized by monoclonal antibodies D3C5 and D3D1 are linear, and correspond to 447–458 and 789–799 amino acids of spike protein of SARS-CoV, respectively. Identification of antigenic epitope of spike protein of SARS-CoV could provide the basis for the development of immunity-based prophylactic, therapeutic, and diagnostic techniques for the control of severe acute respiratory syndrome.
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spelling pubmed-71111542020-04-02 Identification of two antigenic epitopes on SARS-CoV spike protein Hua, Ronghong Zhou, Yanjun Wang, Yunfeng Hua, Yuzhuo Tong, Guangzhi Biochem Biophys Res Commun Article The spike (S) protein of severe acute respiratory syndrome-coronavirus (SARS-CoV) is a major virion structural protein. It plays an important role in interaction with receptor and inducing neutralizing antibodies. In the study, six tentative antigenic epitopes (S1 S2 S3 S4 S5 S6) of the spike protein of SARS-CoV were predicted by bio-informatics analysis, and a multi-epitope chimeric gene of S1–S2–S3–S4–S5–S6 was synthesized and fused to downstream GST gene in pGEX-6p-1. The Western blotting demonstrated that SARS patient convalescent serum could recognize the recombinant fusion protein. A number of monoclonal antibodies were developed against the fusion protein. In further, the six predicted epitope genes were individually fused to GST of pGEX-6p-1 and expressed in Escherichia coli BL21, respectively. Among six fusion peptides, S5 reacted with monoclonal antibody D3C5 and S2 reacted with monoclonal antibody D3D1 against spike protein of SARS-CoV. The epitopes recognized by monoclonal antibodies D3C5 and D3D1 are linear, and correspond to 447–458 and 789–799 amino acids of spike protein of SARS-CoV, respectively. Identification of antigenic epitope of spike protein of SARS-CoV could provide the basis for the development of immunity-based prophylactic, therapeutic, and diagnostic techniques for the control of severe acute respiratory syndrome. Elsevier Inc. 2004-07-02 2004-05-28 /pmc/articles/PMC7111154/ /pubmed/15184071 http://dx.doi.org/10.1016/j.bbrc.2004.05.066 Text en Copyright © 2004 Elsevier Inc. All rights reserved. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active.
spellingShingle Article
Hua, Ronghong
Zhou, Yanjun
Wang, Yunfeng
Hua, Yuzhuo
Tong, Guangzhi
Identification of two antigenic epitopes on SARS-CoV spike protein
title Identification of two antigenic epitopes on SARS-CoV spike protein
title_full Identification of two antigenic epitopes on SARS-CoV spike protein
title_fullStr Identification of two antigenic epitopes on SARS-CoV spike protein
title_full_unstemmed Identification of two antigenic epitopes on SARS-CoV spike protein
title_short Identification of two antigenic epitopes on SARS-CoV spike protein
title_sort identification of two antigenic epitopes on sars-cov spike protein
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7111154/
https://www.ncbi.nlm.nih.gov/pubmed/15184071
http://dx.doi.org/10.1016/j.bbrc.2004.05.066
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