Pocket Contrastive Learning and Conformation Fusion for Robust Structure-Conditioned 3D Molecular Generation under Receptor Conformational Variation.
MOTIVATION: Pocket-conditioned molecular generation incorporates the three-dimensional geometry and chemical environment of protein binding sites into molecular design. However, receptor conformational variation can introduce distribution shifts between training and inference, particularly under cross-docking conditions. Existing approaches often do not fully exploit the correspondence between related receptor conformations during training. RESULTS: We propose a structure-conditioned 3D molecular generation framework that combines pocket-level contrastive learning with reference-conformation feature fusion. Built on a stepwise constructive generative model, these training-stage components encourage stable pocket representations across related conformations while preserving single-pocket inference without requiring a reference conformation. Evaluation on CrossDocked2020 and three external datasets, ASB-E, DUD-E, and APObind, demonstrates improvements in generation success, structural validity, and docking-related performance, particularly under cross-dock evaluation. These results support improved robustness of pocket-conditioned molecular generation under receptor conformational variation. AVAILABILITY AND IMPLEMENTATION: The source code and reproduction instructions are available at https://github.com/LHHHHuan/MTMGen. Pretrained models and an archival code snapshot are available at https://doi.org/10.5281/zenodo.21944857. SUPPLEMENTARY INFORMATION: None.
Authors
- Yijie Ding (ORCID: https://orcid.org/0000-0003-2911-7643)
- Huan Liu
- Hongjie Wu (ORCID: https://orcid.org/0000-0001-5921-8707)
- Xiaoyi Guo
Institutions
- Harbin Institute of Technology (CN)
- Suzhou University of Science and Technology (CN)
- University of Hong Kong (HK)
Publication Details
- Journal
- PubMed
- Published
- 2026-10-05
- DOI
- https://doi.org/10.1093/bioinformatics/btag740
- Primary Topic
- Computational Drug Discovery Methods
- Type
- article
- Field-Weighted Citation Impact
- 0.00