Generative models for structure-based drug design are often limited to a specific modality, restricting their broader applicability. To address this challenge, we introduce FuncBind, a framework based on computer vision to generate target-conditioned, all-atom molecules across atomic systems. FuncBind uses neural fields to represent molecules as continuous atomic densities and employs score-based generative models with modern architectures adapted from the computer vision literature. This modality-agnostic representation allows a single unified model to be trained on diverse atomic systems, from small to large molecules, and handle variable atom/residue counts, including non-canonical amino acids. FuncBind achieves competitive in silico performance in generating small molecules, macrocyclic peptides, and antibody complementarity-determining region loops, conditioned on target structures. FuncBind also generated in vitro novel antibody binders via de novo redesign of the complementarity-determining region H3 loop of two chosen co-crystal structures. As a final contribution, we introduce a new dataset and benchmark for structure-conditioned macrocyclic peptide generation. The code is available at https://github.com/prescient-design/funcbind.
Unified all-atom molecule generation with neural fields
FuncBind, a framework using neural fields and score-based generative models from computer vision, generates diverse atomic structures across modalities, achieving competitive performance in structure-conditioned molecular design.
- Year
- 2025
- Venue
- arXiv 2025
- Authors
- 10
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- Abstract onlyARXIV-DEFAULT
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- arxiv.org/abs/2511.15906ARXIV-DEFAULT
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