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Toward real-world automated antibody design with combinatorial Bayesian optimization

Antibodies are multimeric proteins capable of highly specific molecular recognition. The complementarity determining region 3 of the antibody variable heavy chain (CDRH3) often dominates antigen-binding specificity. Hence, it is a priority to design optimal antigen-specific CDRH3 to develop therapeu...

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Autores principales: Khan, Asif, Cowen-Rivers, Alexander I., Grosnit, Antoine, Deik, Derrick-Goh-Xin, Robert, Philippe A., Greiff, Victor, Smorodina, Eva, Rawat, Puneet, Akbar, Rahmad, Dreczkowski, Kamil, Tutunov, Rasul, Bou-Ammar, Dany, Wang, Jun, Storkey, Amos, Bou-Ammar, Haitham
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939385/
https://www.ncbi.nlm.nih.gov/pubmed/36814835
http://dx.doi.org/10.1016/j.crmeth.2022.100374
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author Khan, Asif
Cowen-Rivers, Alexander I.
Grosnit, Antoine
Deik, Derrick-Goh-Xin
Robert, Philippe A.
Greiff, Victor
Smorodina, Eva
Rawat, Puneet
Akbar, Rahmad
Dreczkowski, Kamil
Tutunov, Rasul
Bou-Ammar, Dany
Wang, Jun
Storkey, Amos
Bou-Ammar, Haitham
author_facet Khan, Asif
Cowen-Rivers, Alexander I.
Grosnit, Antoine
Deik, Derrick-Goh-Xin
Robert, Philippe A.
Greiff, Victor
Smorodina, Eva
Rawat, Puneet
Akbar, Rahmad
Dreczkowski, Kamil
Tutunov, Rasul
Bou-Ammar, Dany
Wang, Jun
Storkey, Amos
Bou-Ammar, Haitham
author_sort Khan, Asif
collection PubMed
description Antibodies are multimeric proteins capable of highly specific molecular recognition. The complementarity determining region 3 of the antibody variable heavy chain (CDRH3) often dominates antigen-binding specificity. Hence, it is a priority to design optimal antigen-specific CDRH3 to develop therapeutic antibodies. The combinatorial structure of CDRH3 sequences makes it impossible to query binding-affinity oracles exhaustively. Moreover, antibodies are expected to have high target specificity and developability. Here, we present AntBO, a combinatorial Bayesian optimization framework utilizing a CDRH3 trust region for an in silico design of antibodies with favorable developability scores. The in silico experiments on 159 antigens demonstrate that AntBO is a step toward practically viable in vitro antibody design. In under 200 calls to the oracle, AntBO suggests antibodies outperforming the best binding sequence from 6.9 million experimentally obtained CDRH3s. Additionally, AntBO finds very-high-affinity CDRH3 in only 38 protein designs while requiring no domain knowledge.
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spelling pubmed-99393852023-02-21 Toward real-world automated antibody design with combinatorial Bayesian optimization Khan, Asif Cowen-Rivers, Alexander I. Grosnit, Antoine Deik, Derrick-Goh-Xin Robert, Philippe A. Greiff, Victor Smorodina, Eva Rawat, Puneet Akbar, Rahmad Dreczkowski, Kamil Tutunov, Rasul Bou-Ammar, Dany Wang, Jun Storkey, Amos Bou-Ammar, Haitham Cell Rep Methods Article Antibodies are multimeric proteins capable of highly specific molecular recognition. The complementarity determining region 3 of the antibody variable heavy chain (CDRH3) often dominates antigen-binding specificity. Hence, it is a priority to design optimal antigen-specific CDRH3 to develop therapeutic antibodies. The combinatorial structure of CDRH3 sequences makes it impossible to query binding-affinity oracles exhaustively. Moreover, antibodies are expected to have high target specificity and developability. Here, we present AntBO, a combinatorial Bayesian optimization framework utilizing a CDRH3 trust region for an in silico design of antibodies with favorable developability scores. The in silico experiments on 159 antigens demonstrate that AntBO is a step toward practically viable in vitro antibody design. In under 200 calls to the oracle, AntBO suggests antibodies outperforming the best binding sequence from 6.9 million experimentally obtained CDRH3s. Additionally, AntBO finds very-high-affinity CDRH3 in only 38 protein designs while requiring no domain knowledge. Elsevier 2023-01-03 /pmc/articles/PMC9939385/ /pubmed/36814835 http://dx.doi.org/10.1016/j.crmeth.2022.100374 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Article
Khan, Asif
Cowen-Rivers, Alexander I.
Grosnit, Antoine
Deik, Derrick-Goh-Xin
Robert, Philippe A.
Greiff, Victor
Smorodina, Eva
Rawat, Puneet
Akbar, Rahmad
Dreczkowski, Kamil
Tutunov, Rasul
Bou-Ammar, Dany
Wang, Jun
Storkey, Amos
Bou-Ammar, Haitham
Toward real-world automated antibody design with combinatorial Bayesian optimization
title Toward real-world automated antibody design with combinatorial Bayesian optimization
title_full Toward real-world automated antibody design with combinatorial Bayesian optimization
title_fullStr Toward real-world automated antibody design with combinatorial Bayesian optimization
title_full_unstemmed Toward real-world automated antibody design with combinatorial Bayesian optimization
title_short Toward real-world automated antibody design with combinatorial Bayesian optimization
title_sort toward real-world automated antibody design with combinatorial bayesian optimization
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9939385/
https://www.ncbi.nlm.nih.gov/pubmed/36814835
http://dx.doi.org/10.1016/j.crmeth.2022.100374
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