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Stepwise prediction and statistical screening: B-cell epitopes on neuraminidase of human avian H(5)N(1) virus
The B-cell epitopes of virus are associated with the antiviral drug and the vaccine screening. As the nucleotide sequences of neuraminidase (NA) of stain GD-01-06 were sequenced, we predicted the α-helix and β-fold structure and the indexes of the flexible regions of secondary structure of NA with m...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SP Science in China Press
2008
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088991/ https://www.ncbi.nlm.nih.gov/pubmed/32214728 http://dx.doi.org/10.1007/s11434-008-0505-0 |
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author | Huang, Ping Yu, ShouYi Ke, ChangWen |
author_facet | Huang, Ping Yu, ShouYi Ke, ChangWen |
author_sort | Huang, Ping |
collection | PubMed |
description | The B-cell epitopes of virus are associated with the antiviral drug and the vaccine screening. As the nucleotide sequences of neuraminidase (NA) of stain GD-01-06 were sequenced, we predicted the α-helix and β-fold structure and the indexes of the flexible regions of secondary structure of NA with methods of the Hydrophilicity plot by Kyte-Doolittle, the Surface probability plot by Emini and the Antigenic index by Jameson-Wolf, and then screened statistically the parameters to predict B-cell epitopes by the Hierarchical cluster and the Bivariate correlation and the quartiles with SPSS 13.0. The impact of variation of amino acids in NA on its epitopes was analyzed. The predictive results were evaluated by Wu’s Antigenic Index and SWISS-MODEL. We found that the most possible epitopes on NA were located within or nearby its N-terminal Nos. 120–137, 81–84, 408–415, 273–282, 429–432, 356–368, 46–55, 146–155, 341–350 and 198–209, which were the dominant regions of NA epitopes. Peptide 120–137 including the glycoprotein domain (NGT(126–128)) was first chosen as the B-cell epitopes on NA. NA in H(5)N(1) strain isolated after 2003 lacked in No. 53 amino acid (I), resulting in an increase in the surface flexible region of NA in GD-01-06 and an enlargement to their epitope regions (VEP(46–48) → VEPISNTNFL(46–55)). Conclusively, prediction of the B-cell epitopes on the NA based on multiple parameters is useful for researches on the molecular immunology and drug screening and immuno-prophylaxis. A deletion of No. 53 amino acid (I) in NA in strain GD-01-06 might increase its antigenicity. |
format | Online Article Text |
id | pubmed-7088991 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | SP Science in China Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-70889912020-03-23 Stepwise prediction and statistical screening: B-cell epitopes on neuraminidase of human avian H(5)N(1) virus Huang, Ping Yu, ShouYi Ke, ChangWen Chin Sci Bull Articles/Immunology The B-cell epitopes of virus are associated with the antiviral drug and the vaccine screening. As the nucleotide sequences of neuraminidase (NA) of stain GD-01-06 were sequenced, we predicted the α-helix and β-fold structure and the indexes of the flexible regions of secondary structure of NA with methods of the Hydrophilicity plot by Kyte-Doolittle, the Surface probability plot by Emini and the Antigenic index by Jameson-Wolf, and then screened statistically the parameters to predict B-cell epitopes by the Hierarchical cluster and the Bivariate correlation and the quartiles with SPSS 13.0. The impact of variation of amino acids in NA on its epitopes was analyzed. The predictive results were evaluated by Wu’s Antigenic Index and SWISS-MODEL. We found that the most possible epitopes on NA were located within or nearby its N-terminal Nos. 120–137, 81–84, 408–415, 273–282, 429–432, 356–368, 46–55, 146–155, 341–350 and 198–209, which were the dominant regions of NA epitopes. Peptide 120–137 including the glycoprotein domain (NGT(126–128)) was first chosen as the B-cell epitopes on NA. NA in H(5)N(1) strain isolated after 2003 lacked in No. 53 amino acid (I), resulting in an increase in the surface flexible region of NA in GD-01-06 and an enlargement to their epitope regions (VEP(46–48) → VEPISNTNFL(46–55)). Conclusively, prediction of the B-cell epitopes on the NA based on multiple parameters is useful for researches on the molecular immunology and drug screening and immuno-prophylaxis. A deletion of No. 53 amino acid (I) in NA in strain GD-01-06 might increase its antigenicity. SP Science in China Press 2008-11-28 2008 /pmc/articles/PMC7088991/ /pubmed/32214728 http://dx.doi.org/10.1007/s11434-008-0505-0 Text en © Science in China Press and Springer-Verlag GmbH 2008 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 | Articles/Immunology Huang, Ping Yu, ShouYi Ke, ChangWen Stepwise prediction and statistical screening: B-cell epitopes on neuraminidase of human avian H(5)N(1) virus |
title | Stepwise prediction and statistical screening: B-cell epitopes on neuraminidase of human avian H(5)N(1) virus |
title_full | Stepwise prediction and statistical screening: B-cell epitopes on neuraminidase of human avian H(5)N(1) virus |
title_fullStr | Stepwise prediction and statistical screening: B-cell epitopes on neuraminidase of human avian H(5)N(1) virus |
title_full_unstemmed | Stepwise prediction and statistical screening: B-cell epitopes on neuraminidase of human avian H(5)N(1) virus |
title_short | Stepwise prediction and statistical screening: B-cell epitopes on neuraminidase of human avian H(5)N(1) virus |
title_sort | stepwise prediction and statistical screening: b-cell epitopes on neuraminidase of human avian h(5)n(1) virus |
topic | Articles/Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7088991/ https://www.ncbi.nlm.nih.gov/pubmed/32214728 http://dx.doi.org/10.1007/s11434-008-0505-0 |
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