AntibodyFlow: Normalizing Flow Model for Designing Antibody Complementarity-Determining Regions

Fuente: arXiv
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Autores principales: Xu, Bohao, Wang, Yanbo, Chen, Wenyu, Shan, Shimin
Formato: Preprint
Publicado: 2024
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author Xu, Bohao
Wang, Yanbo
Chen, Wenyu
Shan, Shimin
author_facet Xu, Bohao
Wang, Yanbo
Chen, Wenyu
Shan, Shimin
contents Therapeutic antibodies have been extensively studied in drug discovery and development in the past decades. Antibodies are specialized protective proteins that bind to antigens in a lock-to-key manner. The binding strength/affinity between an antibody and a specific antigen is heavily determined by the complementarity-determining regions (CDRs) on the antibodies. Existing machine learning methods cast in silico development of CDRs as either sequence or 3D graph (with a single chain) generation tasks and have achieved initial success. However, with CDR loops having specific geometry shapes, learning the 3D geometric structures of CDRs remains a challenge. To address this issue, we propose AntibodyFlow, a 3D flow model to design antibody CDR loops. Specifically, AntibodyFlow first constructs the distance matrix, then predicts amino acids conditioned on the distance matrix. Also, AntibodyFlow conducts constraint learning and constrained generation to ensure valid 3D structures. Experimental results indicate that AntibodyFlow outperforms the best baseline consistently with up to 16.0% relative improvement in validity rate and 24.3% relative reduction in geometric graph level error (root mean square deviation, RMSD).
format Preprint
id arxiv_https___arxiv_org_abs_2406_13162
institution arXiv
publishDate 2024
record_format arxiv
spellingShingle AntibodyFlow: Normalizing Flow Model for Designing Antibody Complementarity-Determining Regions
Xu, Bohao
Wang, Yanbo
Chen, Wenyu
Shan, Shimin
Machine Learning
Artificial Intelligence
Quantitative Methods
Therapeutic antibodies have been extensively studied in drug discovery and development in the past decades. Antibodies are specialized protective proteins that bind to antigens in a lock-to-key manner. The binding strength/affinity between an antibody and a specific antigen is heavily determined by the complementarity-determining regions (CDRs) on the antibodies. Existing machine learning methods cast in silico development of CDRs as either sequence or 3D graph (with a single chain) generation tasks and have achieved initial success. However, with CDR loops having specific geometry shapes, learning the 3D geometric structures of CDRs remains a challenge. To address this issue, we propose AntibodyFlow, a 3D flow model to design antibody CDR loops. Specifically, AntibodyFlow first constructs the distance matrix, then predicts amino acids conditioned on the distance matrix. Also, AntibodyFlow conducts constraint learning and constrained generation to ensure valid 3D structures. Experimental results indicate that AntibodyFlow outperforms the best baseline consistently with up to 16.0% relative improvement in validity rate and 24.3% relative reduction in geometric graph level error (root mean square deviation, RMSD).
title AntibodyFlow: Normalizing Flow Model for Designing Antibody Complementarity-Determining Regions
topic Machine Learning
Artificial Intelligence
Quantitative Methods
url https://arxiv.org/abs/2406.13162