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Identification of a novel linear B-cell epitope in the M protein of avian infectious bronchitis coronaviruses
This report describes the identification of a novel linear B-cell epitope at the C-terminus of the membrane (M) protein of avian infectious bronchitis virus (IBV). A monoclonal antibody (MAb) (designated as 15E2) against the IBV M protein was prepared and a series of 14 partially-overlapping fragmen...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Microbiological Society of Korea
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090873/ https://www.ncbi.nlm.nih.gov/pubmed/19851732 http://dx.doi.org/10.1007/s12275-009-0104-z |
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author | Xing, Junji Liu, Shengwang Han, Zongxi Shao, Yuhao Li, Huixin Kong, Xiangang |
author_facet | Xing, Junji Liu, Shengwang Han, Zongxi Shao, Yuhao Li, Huixin Kong, Xiangang |
author_sort | Xing, Junji |
collection | PubMed |
description | This report describes the identification of a novel linear B-cell epitope at the C-terminus of the membrane (M) protein of avian infectious bronchitis virus (IBV). A monoclonal antibody (MAb) (designated as 15E2) against the IBV M protein was prepared and a series of 14 partially-overlapping fragments of the IBV M gene were expressed with a GST tag. These peptides were subjected to enzyme-linked immunosorbent assay (ELISA) and western blotting analysis using MAb 15E2 to identify the epitope. A linear motif, (199)FATFVYAK(206), which was located at the C-terminus of the M protein, was identified by MAb 15E2. ELISA and western blotting also showed that this epitope could be recognized by IBV-positive serum from chicken. Given that 15E2 showed reactivity with the (199)FATFVYAK(206) motif, expressed as a GST fusion protein, in both western blotting and in an ELISA, we proposed that this motif represented a linear B-cell epitope of the M protein. The (199)FATFVYAK(206) motif was the minimal requirement for reactivity as demonstrated by analysis of the reactivity of 15E2 with several truncated peptides that were derived from the motif. Alignment and comparison of the 15E2-defined epitope sequence with the sequences of other corona-viruses indicated that the epitope is well conserved among chicken and turkey coronaviruses. The identified epitope should be useful in clinical applications and as a tool for the further study of the structure and function of the M protein of IBV. |
format | Online Article Text |
id | pubmed-7090873 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | The Microbiological Society of Korea |
record_format | MEDLINE/PubMed |
spelling | pubmed-70908732020-03-24 Identification of a novel linear B-cell epitope in the M protein of avian infectious bronchitis coronaviruses Xing, Junji Liu, Shengwang Han, Zongxi Shao, Yuhao Li, Huixin Kong, Xiangang J Microbiol Article This report describes the identification of a novel linear B-cell epitope at the C-terminus of the membrane (M) protein of avian infectious bronchitis virus (IBV). A monoclonal antibody (MAb) (designated as 15E2) against the IBV M protein was prepared and a series of 14 partially-overlapping fragments of the IBV M gene were expressed with a GST tag. These peptides were subjected to enzyme-linked immunosorbent assay (ELISA) and western blotting analysis using MAb 15E2 to identify the epitope. A linear motif, (199)FATFVYAK(206), which was located at the C-terminus of the M protein, was identified by MAb 15E2. ELISA and western blotting also showed that this epitope could be recognized by IBV-positive serum from chicken. Given that 15E2 showed reactivity with the (199)FATFVYAK(206) motif, expressed as a GST fusion protein, in both western blotting and in an ELISA, we proposed that this motif represented a linear B-cell epitope of the M protein. The (199)FATFVYAK(206) motif was the minimal requirement for reactivity as demonstrated by analysis of the reactivity of 15E2 with several truncated peptides that were derived from the motif. Alignment and comparison of the 15E2-defined epitope sequence with the sequences of other corona-viruses indicated that the epitope is well conserved among chicken and turkey coronaviruses. The identified epitope should be useful in clinical applications and as a tool for the further study of the structure and function of the M protein of IBV. The Microbiological Society of Korea 2009-10-24 2009 /pmc/articles/PMC7090873/ /pubmed/19851732 http://dx.doi.org/10.1007/s12275-009-0104-z Text en © The Microbiological Society of Korea and Springer Berlin Heidelberg 2009 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Article Xing, Junji Liu, Shengwang Han, Zongxi Shao, Yuhao Li, Huixin Kong, Xiangang Identification of a novel linear B-cell epitope in the M protein of avian infectious bronchitis coronaviruses |
title | Identification of a novel linear B-cell epitope in the M protein of avian infectious bronchitis coronaviruses |
title_full | Identification of a novel linear B-cell epitope in the M protein of avian infectious bronchitis coronaviruses |
title_fullStr | Identification of a novel linear B-cell epitope in the M protein of avian infectious bronchitis coronaviruses |
title_full_unstemmed | Identification of a novel linear B-cell epitope in the M protein of avian infectious bronchitis coronaviruses |
title_short | Identification of a novel linear B-cell epitope in the M protein of avian infectious bronchitis coronaviruses |
title_sort | identification of a novel linear b-cell epitope in the m protein of avian infectious bronchitis coronaviruses |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7090873/ https://www.ncbi.nlm.nih.gov/pubmed/19851732 http://dx.doi.org/10.1007/s12275-009-0104-z |
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