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AbAgIntPre: A deep learning method for predicting antibody-antigen interactions based on sequence information
INTRODUCTION: Antibody-mediated immunity is an essential part of the immune system in vertebrates. The ability to specifically bind to antigens allows antibodies to be widely used in the therapy of cancers and other critical diseases. A key step in antibody therapeutics is the experimental identific...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813736/ https://www.ncbi.nlm.nih.gov/pubmed/36618397 http://dx.doi.org/10.3389/fimmu.2022.1053617 |
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author | Huang, Yan Zhang, Ziding Zhou, Yuan |
author_facet | Huang, Yan Zhang, Ziding Zhou, Yuan |
author_sort | Huang, Yan |
collection | PubMed |
description | INTRODUCTION: Antibody-mediated immunity is an essential part of the immune system in vertebrates. The ability to specifically bind to antigens allows antibodies to be widely used in the therapy of cancers and other critical diseases. A key step in antibody therapeutics is the experimental identification of antibody-antigen interactions, which is generally time-consuming, costly, and laborious. Although some computational methods have been proposed to screen potential antibodies, the dependence on 3D structures still limits the application of these methods. METHODS: Here, we developed a deep learning-assisted prediction method (i.e., AbAgIntPre) for fast identification of antibody-antigen interactions that only relies on amino acid sequences. A Siamese-like convolutional neural network architecture was established with the amino acid composition encoding scheme for both antigens and antibodies. RESULTS AND DISCUSSION: The generic model of AbAgIntPre achieved satisfactory performance with the Area Under Curve (AUC) of 0.82 on a high-quality generic independent test dataset. Besides, this approach also showed competitive performance on the more specific SARS-CoV dataset. We expect that AbAgIntPre can serve as an important complement to traditional experimental methods for antibody screening and effectively reduce the workload of antibody design. The web server of AbAgIntPre is freely available at http://www.zzdlab.com/AbAgIntPre. |
format | Online Article Text |
id | pubmed-9813736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-98137362023-01-06 AbAgIntPre: A deep learning method for predicting antibody-antigen interactions based on sequence information Huang, Yan Zhang, Ziding Zhou, Yuan Front Immunol Immunology INTRODUCTION: Antibody-mediated immunity is an essential part of the immune system in vertebrates. The ability to specifically bind to antigens allows antibodies to be widely used in the therapy of cancers and other critical diseases. A key step in antibody therapeutics is the experimental identification of antibody-antigen interactions, which is generally time-consuming, costly, and laborious. Although some computational methods have been proposed to screen potential antibodies, the dependence on 3D structures still limits the application of these methods. METHODS: Here, we developed a deep learning-assisted prediction method (i.e., AbAgIntPre) for fast identification of antibody-antigen interactions that only relies on amino acid sequences. A Siamese-like convolutional neural network architecture was established with the amino acid composition encoding scheme for both antigens and antibodies. RESULTS AND DISCUSSION: The generic model of AbAgIntPre achieved satisfactory performance with the Area Under Curve (AUC) of 0.82 on a high-quality generic independent test dataset. Besides, this approach also showed competitive performance on the more specific SARS-CoV dataset. We expect that AbAgIntPre can serve as an important complement to traditional experimental methods for antibody screening and effectively reduce the workload of antibody design. The web server of AbAgIntPre is freely available at http://www.zzdlab.com/AbAgIntPre. Frontiers Media S.A. 2022-12-22 /pmc/articles/PMC9813736/ /pubmed/36618397 http://dx.doi.org/10.3389/fimmu.2022.1053617 Text en Copyright © 2022 Huang, Zhang and Zhou https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Huang, Yan Zhang, Ziding Zhou, Yuan AbAgIntPre: A deep learning method for predicting antibody-antigen interactions based on sequence information |
title | AbAgIntPre: A deep learning method for predicting antibody-antigen interactions based on sequence information |
title_full | AbAgIntPre: A deep learning method for predicting antibody-antigen interactions based on sequence information |
title_fullStr | AbAgIntPre: A deep learning method for predicting antibody-antigen interactions based on sequence information |
title_full_unstemmed | AbAgIntPre: A deep learning method for predicting antibody-antigen interactions based on sequence information |
title_short | AbAgIntPre: A deep learning method for predicting antibody-antigen interactions based on sequence information |
title_sort | abagintpre: a deep learning method for predicting antibody-antigen interactions based on sequence information |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9813736/ https://www.ncbi.nlm.nih.gov/pubmed/36618397 http://dx.doi.org/10.3389/fimmu.2022.1053617 |
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