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Identification of a Conserved Linear B-Cell Epitope of Streptococcus dysgalactiae GapC Protein by Screening Phage-Displayed Random Peptide Library

The GapC of Streptococcus dysgalactiae (S. dysgalactiae) is a highly conserved surface protein that can induce protective humoral immune response in animals. However, B-cell epitopes on the S. dysgalactiae GapC have not been well identified. In this study, a monoclonal antibody (mAb5B7) against the...

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Autores principales: Zhang, Limeng, Zhang, Hua, Fan, Ziyao, Zhou, Xue, Yu, Liquan, Sun, Hunan, Wu, Zhijun, Yu, Yongzhong, Song, Baifen, Ma, Jinzhu, Tong, Chunyu, Wang, Xintong, Zhu, Zhanbo, Cui, Yudong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486725/
https://www.ncbi.nlm.nih.gov/pubmed/26121648
http://dx.doi.org/10.1371/journal.pone.0131221
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author Zhang, Limeng
Zhang, Hua
Fan, Ziyao
Zhou, Xue
Yu, Liquan
Sun, Hunan
Wu, Zhijun
Yu, Yongzhong
Song, Baifen
Ma, Jinzhu
Tong, Chunyu
Wang, Xintong
Zhu, Zhanbo
Cui, Yudong
author_facet Zhang, Limeng
Zhang, Hua
Fan, Ziyao
Zhou, Xue
Yu, Liquan
Sun, Hunan
Wu, Zhijun
Yu, Yongzhong
Song, Baifen
Ma, Jinzhu
Tong, Chunyu
Wang, Xintong
Zhu, Zhanbo
Cui, Yudong
author_sort Zhang, Limeng
collection PubMed
description The GapC of Streptococcus dysgalactiae (S. dysgalactiae) is a highly conserved surface protein that can induce protective humoral immune response in animals. However, B-cell epitopes on the S. dysgalactiae GapC have not been well identified. In this study, a monoclonal antibody (mAb5B7) against the GapC(1-150) protein was prepared. After passive transfer, mAb5B7 could partially protect mice against S. dysgalactiae infection. Eleven positive phage clones recognized by mAb5B7 were identified by screening phage-displayed random 12-peptide library, most of which matched the consensus motif DTTQGRFD. The motif sequence exactly matches amino acids 48-55 of the S. dysgalactiae GapC protein. In addition, the motif (48)DTTQGRFD(55) shows high homology among various streptococcus species. Site-directed mutagenic analysis further confirmed that residues D48, T50, Q51, G52 and F54 formed the core motif of (48)DTTQGRFD(55). This motif was the minimal determinant of the B-cell epitope recognized by the mAb5B7. As expected, epitope-peptide evoked protective immune response against S. dysgalactiae infection in immunized mice. Taken together, this identified conserved B-cell epitope within S. dysgalactiae GapC could provide very valuable insights for vaccine design against S. dysgalactiae infection.
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spelling pubmed-44867252015-07-02 Identification of a Conserved Linear B-Cell Epitope of Streptococcus dysgalactiae GapC Protein by Screening Phage-Displayed Random Peptide Library Zhang, Limeng Zhang, Hua Fan, Ziyao Zhou, Xue Yu, Liquan Sun, Hunan Wu, Zhijun Yu, Yongzhong Song, Baifen Ma, Jinzhu Tong, Chunyu Wang, Xintong Zhu, Zhanbo Cui, Yudong PLoS One Research Article The GapC of Streptococcus dysgalactiae (S. dysgalactiae) is a highly conserved surface protein that can induce protective humoral immune response in animals. However, B-cell epitopes on the S. dysgalactiae GapC have not been well identified. In this study, a monoclonal antibody (mAb5B7) against the GapC(1-150) protein was prepared. After passive transfer, mAb5B7 could partially protect mice against S. dysgalactiae infection. Eleven positive phage clones recognized by mAb5B7 were identified by screening phage-displayed random 12-peptide library, most of which matched the consensus motif DTTQGRFD. The motif sequence exactly matches amino acids 48-55 of the S. dysgalactiae GapC protein. In addition, the motif (48)DTTQGRFD(55) shows high homology among various streptococcus species. Site-directed mutagenic analysis further confirmed that residues D48, T50, Q51, G52 and F54 formed the core motif of (48)DTTQGRFD(55). This motif was the minimal determinant of the B-cell epitope recognized by the mAb5B7. As expected, epitope-peptide evoked protective immune response against S. dysgalactiae infection in immunized mice. Taken together, this identified conserved B-cell epitope within S. dysgalactiae GapC could provide very valuable insights for vaccine design against S. dysgalactiae infection. Public Library of Science 2015-06-29 /pmc/articles/PMC4486725/ /pubmed/26121648 http://dx.doi.org/10.1371/journal.pone.0131221 Text en © 2015 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Zhang, Limeng
Zhang, Hua
Fan, Ziyao
Zhou, Xue
Yu, Liquan
Sun, Hunan
Wu, Zhijun
Yu, Yongzhong
Song, Baifen
Ma, Jinzhu
Tong, Chunyu
Wang, Xintong
Zhu, Zhanbo
Cui, Yudong
Identification of a Conserved Linear B-Cell Epitope of Streptococcus dysgalactiae GapC Protein by Screening Phage-Displayed Random Peptide Library
title Identification of a Conserved Linear B-Cell Epitope of Streptococcus dysgalactiae GapC Protein by Screening Phage-Displayed Random Peptide Library
title_full Identification of a Conserved Linear B-Cell Epitope of Streptococcus dysgalactiae GapC Protein by Screening Phage-Displayed Random Peptide Library
title_fullStr Identification of a Conserved Linear B-Cell Epitope of Streptococcus dysgalactiae GapC Protein by Screening Phage-Displayed Random Peptide Library
title_full_unstemmed Identification of a Conserved Linear B-Cell Epitope of Streptococcus dysgalactiae GapC Protein by Screening Phage-Displayed Random Peptide Library
title_short Identification of a Conserved Linear B-Cell Epitope of Streptococcus dysgalactiae GapC Protein by Screening Phage-Displayed Random Peptide Library
title_sort identification of a conserved linear b-cell epitope of streptococcus dysgalactiae gapc protein by screening phage-displayed random peptide library
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4486725/
https://www.ncbi.nlm.nih.gov/pubmed/26121648
http://dx.doi.org/10.1371/journal.pone.0131221
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