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DG-Affinity: predicting antigen–antibody affinity with language models from sequences

BACKGROUND: Antibody-mediated immune responses play a crucial role in the immune defense of human body. The evolution of bioengineering has led the progress of antibody-derived drugs, showing promising efficacy in cancer and autoimmune disease therapy. A critical step of this development process is...

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Autores principales: Yuan, Ye, Chen, Qushuo, Mao, Jun, Li, Guipeng, Pan, Xiaoyong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644518/
https://www.ncbi.nlm.nih.gov/pubmed/37957563
http://dx.doi.org/10.1186/s12859-023-05562-z
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author Yuan, Ye
Chen, Qushuo
Mao, Jun
Li, Guipeng
Pan, Xiaoyong
author_facet Yuan, Ye
Chen, Qushuo
Mao, Jun
Li, Guipeng
Pan, Xiaoyong
author_sort Yuan, Ye
collection PubMed
description BACKGROUND: Antibody-mediated immune responses play a crucial role in the immune defense of human body. The evolution of bioengineering has led the progress of antibody-derived drugs, showing promising efficacy in cancer and autoimmune disease therapy. A critical step of this development process is obtaining the affinity between antibodies and their binding antigens. RESULTS: In this study, we introduce a novel sequence-based antigen–antibody affinity prediction method, named DG-Affinity. DG-Affinity uses deep neural networks to efficiently and accurately predict the affinity between antibodies and antigens from sequences, without the need for structural information. The sequences of both the antigen and the antibody are first transformed into embedding vectors by two pre-trained language models, then these embeddings are concatenated into an ConvNeXt framework with a regression task. The results demonstrate the superiority of DG-Affinity over the existing structure-based prediction methods and the sequence-based tools, achieving a Pearson’s correlation of over 0.65 on an independent test dataset. CONCLUSIONS: Compared to the baseline methods, DG-Affinity achieves the best performance and can advance the development of antibody design. It is freely available as an easy-to-use web server at https://www.digitalgeneai.tech/solution/affinity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05562-z.
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spelling pubmed-106445182023-11-13 DG-Affinity: predicting antigen–antibody affinity with language models from sequences Yuan, Ye Chen, Qushuo Mao, Jun Li, Guipeng Pan, Xiaoyong BMC Bioinformatics Research BACKGROUND: Antibody-mediated immune responses play a crucial role in the immune defense of human body. The evolution of bioengineering has led the progress of antibody-derived drugs, showing promising efficacy in cancer and autoimmune disease therapy. A critical step of this development process is obtaining the affinity between antibodies and their binding antigens. RESULTS: In this study, we introduce a novel sequence-based antigen–antibody affinity prediction method, named DG-Affinity. DG-Affinity uses deep neural networks to efficiently and accurately predict the affinity between antibodies and antigens from sequences, without the need for structural information. The sequences of both the antigen and the antibody are first transformed into embedding vectors by two pre-trained language models, then these embeddings are concatenated into an ConvNeXt framework with a regression task. The results demonstrate the superiority of DG-Affinity over the existing structure-based prediction methods and the sequence-based tools, achieving a Pearson’s correlation of over 0.65 on an independent test dataset. CONCLUSIONS: Compared to the baseline methods, DG-Affinity achieves the best performance and can advance the development of antibody design. It is freely available as an easy-to-use web server at https://www.digitalgeneai.tech/solution/affinity. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s12859-023-05562-z. BioMed Central 2023-11-13 /pmc/articles/PMC10644518/ /pubmed/37957563 http://dx.doi.org/10.1186/s12859-023-05562-z Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open Access This 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
Yuan, Ye
Chen, Qushuo
Mao, Jun
Li, Guipeng
Pan, Xiaoyong
DG-Affinity: predicting antigen–antibody affinity with language models from sequences
title DG-Affinity: predicting antigen–antibody affinity with language models from sequences
title_full DG-Affinity: predicting antigen–antibody affinity with language models from sequences
title_fullStr DG-Affinity: predicting antigen–antibody affinity with language models from sequences
title_full_unstemmed DG-Affinity: predicting antigen–antibody affinity with language models from sequences
title_short DG-Affinity: predicting antigen–antibody affinity with language models from sequences
title_sort dg-affinity: predicting antigen–antibody affinity with language models from sequences
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10644518/
https://www.ncbi.nlm.nih.gov/pubmed/37957563
http://dx.doi.org/10.1186/s12859-023-05562-z
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