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ABSTRACT
Despite the central role that antibodies play in modern medicine, there is currently no way to rationally design novel antibodies to bind a specific epitope on a target. Instead, antibody discovery currently involves time-consuming immunization of an animal or library screening approaches. Here we demonstrate that a fine-tuned RFdiffusion network is capable of designing de novo antibody variable heavy chains (VHH's) that bind user-specified epitopes. We experimentally confirm binders to four disease-relevant epitopes, and the cryo-EM structure of a designed VHH bound to influenza hemagglutinin is nearly identical to the design model both in the configuration of the CDR loops and the overall binding pose.
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Full text: Available Collection: Preprints Database: bioRxiv Main subject: Heavy Chain Disease Language: English Year: 2024 Document Type: Preprint

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Full text: Available Collection: Preprints Database: bioRxiv Main subject: Heavy Chain Disease Language: English Year: 2024 Document Type: Preprint