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A Strategy for Searching Antigenic Regions in the SARS-CoV Spike Protein

In the face of the worldwide threat of severe acute respiratory syndrome (SARS) to human life, some of the most urgent challenges are to develop fast and accurate analytical methods for early diagnosis of this disease as well as to create a safe anti-viral vaccine for prevention. To these ends, we i...

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Detalles Bibliográficos
Autores principales: Ren, Yan, Zhou, Zhengfeng, Liu, Jinxiu, Lin, Liang, Li, Shuting, Wang, Hao, Xia, Ji, Zhao, Zhe, Wen, Jie, Zhou, Cuiqi, Wang, Jingqiang, Yin, Jianning, Xu, Ningzhi, Liu, Siqi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172407/
https://www.ncbi.nlm.nih.gov/pubmed/15629033
http://dx.doi.org/10.1016/S1672-0229(03)01026-X
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author Ren, Yan
Zhou, Zhengfeng
Liu, Jinxiu
Lin, Liang
Li, Shuting
Wang, Hao
Xia, Ji
Zhao, Zhe
Wen, Jie
Zhou, Cuiqi
Wang, Jingqiang
Yin, Jianning
Xu, Ningzhi
Liu, Siqi
author_facet Ren, Yan
Zhou, Zhengfeng
Liu, Jinxiu
Lin, Liang
Li, Shuting
Wang, Hao
Xia, Ji
Zhao, Zhe
Wen, Jie
Zhou, Cuiqi
Wang, Jingqiang
Yin, Jianning
Xu, Ningzhi
Liu, Siqi
author_sort Ren, Yan
collection PubMed
description In the face of the worldwide threat of severe acute respiratory syndrome (SARS) to human life, some of the most urgent challenges are to develop fast and accurate analytical methods for early diagnosis of this disease as well as to create a safe anti-viral vaccine for prevention. To these ends, we investigated the antigenicity of the spike protein (S protein), a major structural protein in the SARS-coronavirus (SARS-CoV). Based upon the theoretical analysis for hydrophobicity of the S protein, 18 peptides were synthesized. Using Enzyme-Linked Immunosorbent Assay (ELISA), these peptides were screened in the sera from SARS patients. According to these results, two fragments of the S gene were amplified by PCR and cloned into pET-32a. Both S fragments were expressed in the BL-21 strain and further purified with an affinity chromatography. These recombinant S fragments were confirmed to have positive cross-reactions with SARS sera, either by Western blot or by ELISA. Our results demonstrated that the potential epitope regions were located at Codons 469–882 in the S protein, and one epitope site was located at Codons 599–620. Identification of antigenic regions in the SARS-CoV S protein may be important for the functional studies of this virus or the development of clinical diagnosis.
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spelling pubmed-51724072016-12-23 A Strategy for Searching Antigenic Regions in the SARS-CoV Spike Protein Ren, Yan Zhou, Zhengfeng Liu, Jinxiu Lin, Liang Li, Shuting Wang, Hao Xia, Ji Zhao, Zhe Wen, Jie Zhou, Cuiqi Wang, Jingqiang Yin, Jianning Xu, Ningzhi Liu, Siqi Genomics Proteomics Bioinformatics Invited Article In the face of the worldwide threat of severe acute respiratory syndrome (SARS) to human life, some of the most urgent challenges are to develop fast and accurate analytical methods for early diagnosis of this disease as well as to create a safe anti-viral vaccine for prevention. To these ends, we investigated the antigenicity of the spike protein (S protein), a major structural protein in the SARS-coronavirus (SARS-CoV). Based upon the theoretical analysis for hydrophobicity of the S protein, 18 peptides were synthesized. Using Enzyme-Linked Immunosorbent Assay (ELISA), these peptides were screened in the sera from SARS patients. According to these results, two fragments of the S gene were amplified by PCR and cloned into pET-32a. Both S fragments were expressed in the BL-21 strain and further purified with an affinity chromatography. These recombinant S fragments were confirmed to have positive cross-reactions with SARS sera, either by Western blot or by ELISA. Our results demonstrated that the potential epitope regions were located at Codons 469–882 in the S protein, and one epitope site was located at Codons 599–620. Identification of antigenic regions in the SARS-CoV S protein may be important for the functional studies of this virus or the development of clinical diagnosis. Elsevier 2003-08 2016-11-28 /pmc/articles/PMC5172407/ /pubmed/15629033 http://dx.doi.org/10.1016/S1672-0229(03)01026-X Text en . http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Invited Article
Ren, Yan
Zhou, Zhengfeng
Liu, Jinxiu
Lin, Liang
Li, Shuting
Wang, Hao
Xia, Ji
Zhao, Zhe
Wen, Jie
Zhou, Cuiqi
Wang, Jingqiang
Yin, Jianning
Xu, Ningzhi
Liu, Siqi
A Strategy for Searching Antigenic Regions in the SARS-CoV Spike Protein
title A Strategy for Searching Antigenic Regions in the SARS-CoV Spike Protein
title_full A Strategy for Searching Antigenic Regions in the SARS-CoV Spike Protein
title_fullStr A Strategy for Searching Antigenic Regions in the SARS-CoV Spike Protein
title_full_unstemmed A Strategy for Searching Antigenic Regions in the SARS-CoV Spike Protein
title_short A Strategy for Searching Antigenic Regions in the SARS-CoV Spike Protein
title_sort strategy for searching antigenic regions in the sars-cov spike protein
topic Invited Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5172407/
https://www.ncbi.nlm.nih.gov/pubmed/15629033
http://dx.doi.org/10.1016/S1672-0229(03)01026-X
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