Toward real-world automated antibody design with combinatorial Bayesian optimization

dc.contributor.authorKhan, Asif
dc.contributor.authorCowen-Rivers, Alexander I.
dc.contributor.authorGrosnit, Antoine
dc.contributor.authorDeik, Derrick Goh Xin
dc.contributor.authorRobert, Philippe A.
dc.contributor.authorGreiff, Victor
dc.contributor.authorSmorodina, Eva
dc.contributor.authorRawat, Puneet
dc.contributor.authorAkbar, Rahmad
dc.contributor.authorDreczkowski, Kamil
dc.contributor.authorTutunov, Rasul
dc.contributor.authorBou-Ammar, Dany
dc.contributor.authorWang, Jun
dc.contributor.authorStorkey, Amos J.
dc.contributor.authorAmmar, Haitham Bou
dc.contributor.departmentDepartment of Computer Science
dc.contributor.facultyFaculty of Medicine (FM)
dc.contributor.facultyFaculty of Arts and Sciences (FAS)
dc.contributor.institutionAmerican University of Beirut
dc.date.accessioned2025-01-24T11:23:04Z
dc.date.available2025-01-24T11:23:04Z
dc.date.issued2023
dc.description.abstractAntibodies 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
dc.identifier.doihttps://doi.org/10.1016/j.crmeth.2022.100374
dc.identifier.eid2-s2.0-85146916704
dc.identifier.pmid36814835
dc.identifier.urihttp://hdl.handle.net/10938/25626
dc.language.isoen
dc.publisherCell Press
dc.relation.ispartofCell Reports Methods
dc.sourceScopus
dc.subjectBayesian optimization
dc.subjectCombinatorial bayesian optimization
dc.subjectComputational antibody design
dc.subjectCp: biotechnology
dc.subjectCp: immunology
dc.subjectGaussian processes
dc.subjectMachine learning
dc.subjectProtein engineering
dc.subjectStructural biology
dc.subjectAntibodies
dc.subjectAntigens
dc.subjectBayes theorem
dc.subjectComplementarity determining regions
dc.subjectImmunoglobulin heavy chains
dc.subjectCoronavirus spike glycoprotein
dc.subjectSars-cov-2 antibody
dc.subjectVirus antigen
dc.subjectAntibody
dc.subjectAntigen
dc.subjectImmunoglobulin heavy chain
dc.subjectAmino acid sequence
dc.subjectAntibody detection
dc.subjectArticle
dc.subjectAutoanalysis
dc.subjectBinding affinity
dc.subjectBiophysics
dc.subjectIn vitro study
dc.subjectMutation
dc.subjectNonhuman
dc.subjectSevere acute respiratory syndrome coronavirus 2
dc.subjectVirus entry
dc.subjectChemistry
dc.subjectComplementarity determining region
dc.subjectGenetics
dc.titleToward real-world automated antibody design with combinatorial Bayesian optimization
dc.typeArticle

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