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Precision at Every Scale: Efficiency in AI-Driven De Novo Antibody Design

Hyeonjin Cha, Kyesoo Cho, Jeonghyeon Gu, Daehyeon Gwak, Seung Woo Ham, Mirim Hong, Sehan Kim, Suyeon Kim, Sohee Kwon, Changsoo Lee, Dohoon Lee, Danyeong Lee, Dohoon Lee, Jungsub Lim, Jinsung Noh, Soyeon Oh, Taeyong Park, Seongchan Park, Taeyong Park, Eunwoo Ryu, Seongok Ryu, Deok Hyang Sa, Chaok Seok, Jiho Sim, Moo Young Song, Jonghun Won, Hyeonuk Woo, Jinsol Yang

Discovered via OpenAlex

Abstract

The precise de novo design of antibodies remains a therapeutic challenge. The AI platform, GaluxDesign, was evaluated in a high-efficiency Precision-Scale Workflow by synthesizing and testing only 50 full-length IgG candidates per epitope across eight distinct epitopes from six therapeutic targets. This campaign yielded a 10.5% binder rate (estimated EC 50 < 100 nM), identifying target-specific binders for seven of eight epitopes, with multiple candidates exhibiting sub-nanomolar to single-digit nanomolar dissociation constants (K d ). We further assessed the same workflow on nine shared benchmark targets selected for external comparison, where GaluxDesign identified target-specific binders for eight of nine targets, demonstrating strong target-level performance relative to previously reported de novo antibody design approaches. Together, these results establish a high-efficiency, precision-scale workflow for generating novel, high-affinity therapeutic antibodies.

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