Toward real-world automated antibody design with combinatorial Bayesian optimization

Asif Khan(University of Edinburgh), Alexander I. Cowen-Rivers(Technical University of Darmstadt), Antoine Grosnit(Huawei Technologies (United Kingdom)), Derrick-Goh-Xin Deik(Huawei Technologies (United Kingdom)), Philippe A. Robert(Oslo University Hospital), Victor Greiff(University of Oslo), Eva Smorodina(Oslo University Hospital), Puneet Rawat(Oslo University Hospital), Rahmad Akbar(University of Oslo), Kamil Dreczkowski(Huawei Technologies (United Kingdom)), Rasul Tutunov(Huawei Technologies (United Kingdom)), Dany Bou-Ammar(American University of Beirut Medical Center), Jun Wang(University College London), Amos Storkey(University of Edinburgh), Haitham Bou Ammar(University College London)
Cell Reports Methods
January 1, 2023
Cited by 43Open Access
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Abstract

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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