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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier Inc.
2004
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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. |
format | Online Article Text |
id | pubmed-7111154 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | Elsevier Inc. |
record_format | MEDLINE/PubMed |
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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