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SEPPA 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens
B-cell epitope information is critical to immune therapy and vaccine design. Protein epitopes can be significantly affected by glycosylation, while no methods have considered this till now. Based on previous versions of Spatial Epitope Prediction of Protein Antigens (SEPPA), we here present an enhan...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602482/ https://www.ncbi.nlm.nih.gov/pubmed/31114919 http://dx.doi.org/10.1093/nar/gkz413 |
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author | Zhou, Chen Chen, Zikun Zhang, Lu Yan, Deyu Mao, Tiantian Tang, Kailin Qiu, Tianyi Cao, Zhiwei |
author_facet | Zhou, Chen Chen, Zikun Zhang, Lu Yan, Deyu Mao, Tiantian Tang, Kailin Qiu, Tianyi Cao, Zhiwei |
author_sort | Zhou, Chen |
collection | PubMed |
description | B-cell epitope information is critical to immune therapy and vaccine design. Protein epitopes can be significantly affected by glycosylation, while no methods have considered this till now. Based on previous versions of Spatial Epitope Prediction of Protein Antigens (SEPPA), we here present an enhanced tool SEPPA 3.0, enabling glycoprotein antigens. Parameters were updated based on the latest and largest dataset. Then, additional micro-environmental features of glycosylation triangles and glycosylation-related amino acid indexes were added as important classifiers, coupled with final calibration based on neighboring antigenicity. Logistic regression model was retained as SEPPA 2.0. The AUC value of 0.794 was obtained through 10-fold cross-validation on internal validation. Independent testing on general protein antigens resulted in AUC of 0.740 with BA (balanced accuracy) of 0.657 as baseline of SEPPA 3.0. Most importantly, when tested on independent glycoprotein antigens only, SEPPA 3.0 gave an AUC of 0.749 and BA of 0.665, leading the top performance among peers. As the first server enabling accurate epitope prediction for glycoproteins, SEPPA 3.0 shows significant advantages over popular peers on both general protein and glycoprotein antigens. It can be accessed at http://bidd2.nus.edu.sg/SEPPA3/ or at http://www.badd-cao.net/seppa3/index.html. Batch query is supported. |
format | Online Article Text |
id | pubmed-6602482 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-66024822019-07-05 SEPPA 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens Zhou, Chen Chen, Zikun Zhang, Lu Yan, Deyu Mao, Tiantian Tang, Kailin Qiu, Tianyi Cao, Zhiwei Nucleic Acids Res Web Server Issue B-cell epitope information is critical to immune therapy and vaccine design. Protein epitopes can be significantly affected by glycosylation, while no methods have considered this till now. Based on previous versions of Spatial Epitope Prediction of Protein Antigens (SEPPA), we here present an enhanced tool SEPPA 3.0, enabling glycoprotein antigens. Parameters were updated based on the latest and largest dataset. Then, additional micro-environmental features of glycosylation triangles and glycosylation-related amino acid indexes were added as important classifiers, coupled with final calibration based on neighboring antigenicity. Logistic regression model was retained as SEPPA 2.0. The AUC value of 0.794 was obtained through 10-fold cross-validation on internal validation. Independent testing on general protein antigens resulted in AUC of 0.740 with BA (balanced accuracy) of 0.657 as baseline of SEPPA 3.0. Most importantly, when tested on independent glycoprotein antigens only, SEPPA 3.0 gave an AUC of 0.749 and BA of 0.665, leading the top performance among peers. As the first server enabling accurate epitope prediction for glycoproteins, SEPPA 3.0 shows significant advantages over popular peers on both general protein and glycoprotein antigens. It can be accessed at http://bidd2.nus.edu.sg/SEPPA3/ or at http://www.badd-cao.net/seppa3/index.html. Batch query is supported. Oxford University Press 2019-07-02 2019-05-22 /pmc/articles/PMC6602482/ /pubmed/31114919 http://dx.doi.org/10.1093/nar/gkz413 Text en © The Author(s) 2019. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Web Server Issue Zhou, Chen Chen, Zikun Zhang, Lu Yan, Deyu Mao, Tiantian Tang, Kailin Qiu, Tianyi Cao, Zhiwei SEPPA 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens |
title | SEPPA 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens |
title_full | SEPPA 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens |
title_fullStr | SEPPA 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens |
title_full_unstemmed | SEPPA 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens |
title_short | SEPPA 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens |
title_sort | seppa 3.0—enhanced spatial epitope prediction enabling glycoprotein antigens |
topic | Web Server Issue |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6602482/ https://www.ncbi.nlm.nih.gov/pubmed/31114919 http://dx.doi.org/10.1093/nar/gkz413 |
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