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ImmuneBuilder: Deep-Learning models for predicting the structures of immune proteins
Immune receptor proteins play a key role in the immune system and have shown great promise as biotherapeutics. The structure of these proteins is critical for understanding their antigen binding properties. Here, we present ImmuneBuilder, a set of deep learning models trained to accurately predict t...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227038/ https://www.ncbi.nlm.nih.gov/pubmed/37248282 http://dx.doi.org/10.1038/s42003-023-04927-7 |
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author | Abanades, Brennan Wong, Wing Ki Boyles, Fergus Georges, Guy Bujotzek, Alexander Deane, Charlotte M. |
author_facet | Abanades, Brennan Wong, Wing Ki Boyles, Fergus Georges, Guy Bujotzek, Alexander Deane, Charlotte M. |
author_sort | Abanades, Brennan |
collection | PubMed |
description | Immune receptor proteins play a key role in the immune system and have shown great promise as biotherapeutics. The structure of these proteins is critical for understanding their antigen binding properties. Here, we present ImmuneBuilder, a set of deep learning models trained to accurately predict the structure of antibodies (ABodyBuilder2), nanobodies (NanoBodyBuilder2) and T-Cell receptors (TCRBuilder2). We show that ImmuneBuilder generates structures with state of the art accuracy while being far faster than AlphaFold2. For example, on a benchmark of 34 recently solved antibodies, ABodyBuilder2 predicts CDR-H3 loops with an RMSD of 2.81Å, a 0.09Å improvement over AlphaFold-Multimer, while being over a hundred times faster. Similar results are also achieved for nanobodies, (NanoBodyBuilder2 predicts CDR-H3 loops with an average RMSD of 2.89Å, a 0.55Å improvement over AlphaFold2) and TCRs. By predicting an ensemble of structures, ImmuneBuilder also gives an error estimate for every residue in its final prediction. ImmuneBuilder is made freely available, both to download (https://github.com/oxpig/ImmuneBuilder) and to use via our webserver (http://opig.stats.ox.ac.uk/webapps/newsabdab/sabpred). We also make available structural models for ~150 thousand non-redundant paired antibody sequences (10.5281/zenodo.7258553). |
format | Online Article Text |
id | pubmed-10227038 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-102270382023-05-31 ImmuneBuilder: Deep-Learning models for predicting the structures of immune proteins Abanades, Brennan Wong, Wing Ki Boyles, Fergus Georges, Guy Bujotzek, Alexander Deane, Charlotte M. Commun Biol Article Immune receptor proteins play a key role in the immune system and have shown great promise as biotherapeutics. The structure of these proteins is critical for understanding their antigen binding properties. Here, we present ImmuneBuilder, a set of deep learning models trained to accurately predict the structure of antibodies (ABodyBuilder2), nanobodies (NanoBodyBuilder2) and T-Cell receptors (TCRBuilder2). We show that ImmuneBuilder generates structures with state of the art accuracy while being far faster than AlphaFold2. For example, on a benchmark of 34 recently solved antibodies, ABodyBuilder2 predicts CDR-H3 loops with an RMSD of 2.81Å, a 0.09Å improvement over AlphaFold-Multimer, while being over a hundred times faster. Similar results are also achieved for nanobodies, (NanoBodyBuilder2 predicts CDR-H3 loops with an average RMSD of 2.89Å, a 0.55Å improvement over AlphaFold2) and TCRs. By predicting an ensemble of structures, ImmuneBuilder also gives an error estimate for every residue in its final prediction. ImmuneBuilder is made freely available, both to download (https://github.com/oxpig/ImmuneBuilder) and to use via our webserver (http://opig.stats.ox.ac.uk/webapps/newsabdab/sabpred). We also make available structural models for ~150 thousand non-redundant paired antibody sequences (10.5281/zenodo.7258553). Nature Publishing Group UK 2023-05-29 /pmc/articles/PMC10227038/ /pubmed/37248282 http://dx.doi.org/10.1038/s42003-023-04927-7 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Abanades, Brennan Wong, Wing Ki Boyles, Fergus Georges, Guy Bujotzek, Alexander Deane, Charlotte M. ImmuneBuilder: Deep-Learning models for predicting the structures of immune proteins |
title | ImmuneBuilder: Deep-Learning models for predicting the structures of immune proteins |
title_full | ImmuneBuilder: Deep-Learning models for predicting the structures of immune proteins |
title_fullStr | ImmuneBuilder: Deep-Learning models for predicting the structures of immune proteins |
title_full_unstemmed | ImmuneBuilder: Deep-Learning models for predicting the structures of immune proteins |
title_short | ImmuneBuilder: Deep-Learning models for predicting the structures of immune proteins |
title_sort | immunebuilder: deep-learning models for predicting the structures of immune proteins |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10227038/ https://www.ncbi.nlm.nih.gov/pubmed/37248282 http://dx.doi.org/10.1038/s42003-023-04927-7 |
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