Today, we’re releasing new data showing that Chai-2 can design antibodies against challenging targets with atomic precision.
In June, we introduced Chai-2, showing it could design antibodies zero-shot in a 24-well plate.
In this new data, we show that Chai-2 can:
💡Design full-length mAbs, with >86% of designs showing developability characteristics on par with approved therapeutics, while maintaining the high hit rates we previously reported.
🔬Achieve atomic-level precision on epitope targeting, with Cryo-EM structures matching model designs across five antibody-antigen complexes
🏁 Generate binders and functional agonists against a panel of six GPCRs, which are notoriously hard-to-drug targets. Testing just <75 designs for each, we obtain a binder in every case (median hit rate: 21%). We discover functional agonists to two distinct GPCR targets.
🔎 Design antibodies for peptide-MHC that discriminate single-residue mutations, including binders specific to KRAS G12V over G12D and wild-type peptides
These results provide a glimpse into a new paradigm, where drug designs are conceived on the computer and predictive models approach the precision of the wet lab.
Thank you to many partners for making this possible: Oracle, Mithril, Amazon Web Services (AWS), NVIDIA, Modal for compute; Sino Biological, GenScript for conducting many wet-lab experiments in the paper.