Toward Protein Docking-oriented De Novo Ligand Design via Gradient Inversion

Zekai Chen, Xunkai Li, Sirui Zhang, Henan Sun, Jia Li, Zhenjun Li, Bing Zhou, Rong-Hua Li, Guoren Wang

Keywords: Receptor-Ligand Docking, De Novo Ligand Design, Inversion Framework

Abstract:

De novo ligand design is a fundamental task that seeks to generate protein or molecule candidates that can effectively dock with protein receptors and achieve strong binding affinity entirely from scratch.
It holds paramount significance for a wide spectrum of biomedical applications.
However, most existing studies are constrained by the \textbf{Pseudo De Novo}, \textbf{Limited Docking Modeling}, and \textbf{Inflexible Ligand Type}.
To address these issues, we propose MagicDock, a forward-looking framework grounded in the progressive pipeline and differentiable surface modeling.
(1) We adopt a well-designed gradient inversion framework.
To begin with, general docking knowledge of receptors and ligands is incorporated into the backbone model.
Subsequently, the docking knowledge is instantiated as reverse gradient flows by binding prediction, which iteratively guide the de novo generation of ligands.
(2) We emphasize differentiable surface modeling in the docking process, leveraging learnable 3D point-cloud representations to precisely capture binding details, thereby ensuring that the generated ligands preserve docking validity through direct and interpretable spatial fingerprints.
(3) We introduce customized designs for different ligand types and integrate them into a unified gradient inversion framework with flexible triggers, thereby ensuring broad applicability.
Moreover, we provide rigorous theoretical guarantees for each component of MagicDock.
Extensive experiments across 9 scenarios demonstrate that MagicDock achieves average improvements of 27.1\% and 11.7\% over SOTA baselines specialized for protein or molecule ligand design, respectively.

Primary Area: applications to physical sciences (physics, chemistry, biology, etc.)

Submission Number: 2354