Toward real-world automated antibody design with combinatorial Bayesian optimization
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Cell Press
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. © 2022 The Authors
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Bayesian optimization, Combinatorial bayesian optimization, Computational antibody design, Cp: biotechnology, Cp: immunology, Gaussian processes, Machine learning, Protein engineering, Structural biology, Antibodies, Antigens, Bayes theorem, Complementarity determining regions, Immunoglobulin heavy chains, Coronavirus spike glycoprotein, Sars-cov-2 antibody, Virus antigen, Antibody, Antigen, Immunoglobulin heavy chain, Amino acid sequence, Antibody detection, Article, Autoanalysis, Binding affinity, Biophysics, In vitro study, Mutation, Nonhuman, Severe acute respiratory syndrome coronavirus 2, Virus entry, Chemistry, Complementarity determining region, Genetics