bioRxivBioengineeringPreprint
Precision at Every Scale: Efficiency in AI-Driven De Novo Antibody Design
Hyeonjin Cha, Kyesoo Cho, Jeonghyeon GuiD, Daehyeon Gwak, Seung Woo Ham, Mirim Hong, Sehan Kim, Suyeon Kim, Sohee KwoniD, Changsoo LeeiD, Dohoon LeeiD, Danyeong Lee, Dohoon LeeiD, Jungsub Lim, Jinsung NohiD, Soyeon Oh, Taeyong ParkiD, Seongchan ParkiD, Eunwoo Ryu, Seongok RyuiD, Deok Hyang Sa, Chaok SeokiD, Jiho Sim, Moo Young Song, Jonghun WoniD, , Jinsol YangiD
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 EC50 < 100 nM), identifying target-specific binders for seven of eight epitopes, with multiple candidates exhibiting sub-nanomolar to single-digit nanomolar dissociation constants (Kd). 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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