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Conformational epitope matching and prediction based on protein surface spiral features
BACKGROUND: A conformational epitope (CE) is composed of neighboring amino acid residues located on an antigenic protein surface structure. CEs bind their complementary paratopes in B-cell receptors and/or antibodies. An effective and efficient prediction tool for CE analysis is critical for the dev...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165135/ https://www.ncbi.nlm.nih.gov/pubmed/34058977 http://dx.doi.org/10.1186/s12864-020-07303-5 |
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author | Lo, Ying-Tsang Shih, Tao-Chuan Pai, Tun-Wen Ho, Li-Ping Wu, Jen-Leih Chou, Hsin-Yiu |
author_facet | Lo, Ying-Tsang Shih, Tao-Chuan Pai, Tun-Wen Ho, Li-Ping Wu, Jen-Leih Chou, Hsin-Yiu |
author_sort | Lo, Ying-Tsang |
collection | PubMed |
description | BACKGROUND: A conformational epitope (CE) is composed of neighboring amino acid residues located on an antigenic protein surface structure. CEs bind their complementary paratopes in B-cell receptors and/or antibodies. An effective and efficient prediction tool for CE analysis is critical for the development of immunology-related applications, such as vaccine design and disease diagnosis. RESULTS: We propose a novel method consisting of two sequential modules: matching and prediction. The matching module includes two main approaches. The first approach is a complete sequence search (CSS) that applies BLAST to align the sequence with all known antigen sequences. Fragments with high epitope sequence identities are identified and the predicted residues are annotated on the query structure. The second approach is a spiral vector search (SVS) that adopts a novel surface spiral feature vector for large-scale surface patch detection when queried against a comprehensive epitope database. The prediction module also contains two proposed subsystems. The first system is based on knowledge-based energy and geometrical neighboring residue contents, and the second system adopts combinatorial features, including amino acid contents and physicochemical characteristics, to formulate corresponding geometric spiral vectors and compare them with all spiral vectors from known CEs. An integrated testing dataset was generated for method evaluation, and our two searching methods effectively identified all epitope regions. The prediction results show that our proposed method outperforms previously published systems in terms of sensitivity, specificity, positive predictive value, and accuracy. CONCLUSIONS: The proposed method significantly improves the performance of traditional epitope prediction. Matching followed by prediction is an efficient and effective approach compared to predicting directly on specific surfaces containing antigenic characteristics. |
format | Online Article Text |
id | pubmed-8165135 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-81651352021-06-01 Conformational epitope matching and prediction based on protein surface spiral features Lo, Ying-Tsang Shih, Tao-Chuan Pai, Tun-Wen Ho, Li-Ping Wu, Jen-Leih Chou, Hsin-Yiu BMC Genomics Research BACKGROUND: A conformational epitope (CE) is composed of neighboring amino acid residues located on an antigenic protein surface structure. CEs bind their complementary paratopes in B-cell receptors and/or antibodies. An effective and efficient prediction tool for CE analysis is critical for the development of immunology-related applications, such as vaccine design and disease diagnosis. RESULTS: We propose a novel method consisting of two sequential modules: matching and prediction. The matching module includes two main approaches. The first approach is a complete sequence search (CSS) that applies BLAST to align the sequence with all known antigen sequences. Fragments with high epitope sequence identities are identified and the predicted residues are annotated on the query structure. The second approach is a spiral vector search (SVS) that adopts a novel surface spiral feature vector for large-scale surface patch detection when queried against a comprehensive epitope database. The prediction module also contains two proposed subsystems. The first system is based on knowledge-based energy and geometrical neighboring residue contents, and the second system adopts combinatorial features, including amino acid contents and physicochemical characteristics, to formulate corresponding geometric spiral vectors and compare them with all spiral vectors from known CEs. An integrated testing dataset was generated for method evaluation, and our two searching methods effectively identified all epitope regions. The prediction results show that our proposed method outperforms previously published systems in terms of sensitivity, specificity, positive predictive value, and accuracy. CONCLUSIONS: The proposed method significantly improves the performance of traditional epitope prediction. Matching followed by prediction is an efficient and effective approach compared to predicting directly on specific surfaces containing antigenic characteristics. BioMed Central 2021-05-31 /pmc/articles/PMC8165135/ /pubmed/34058977 http://dx.doi.org/10.1186/s12864-020-07303-5 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Lo, Ying-Tsang Shih, Tao-Chuan Pai, Tun-Wen Ho, Li-Ping Wu, Jen-Leih Chou, Hsin-Yiu Conformational epitope matching and prediction based on protein surface spiral features |
title | Conformational epitope matching and prediction based on protein surface spiral features |
title_full | Conformational epitope matching and prediction based on protein surface spiral features |
title_fullStr | Conformational epitope matching and prediction based on protein surface spiral features |
title_full_unstemmed | Conformational epitope matching and prediction based on protein surface spiral features |
title_short | Conformational epitope matching and prediction based on protein surface spiral features |
title_sort | conformational epitope matching and prediction based on protein surface spiral features |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8165135/ https://www.ncbi.nlm.nih.gov/pubmed/34058977 http://dx.doi.org/10.1186/s12864-020-07303-5 |
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