TY - JOUR
T1 - Target-aware 3D molecular generation based on guided equivariant diffusion
AU - Hu, Qiaoyu
AU - Sun, Changzhi
AU - He, Huan
AU - Xu, Jiazheng
AU - Liu, Danlin
AU - Zhang, Wenqing
AU - Shi, Sumeng
AU - Zhang, Kai
AU - Li, Honglin
N1 - Publisher Copyright:
© The Author(s) 2025.
PY - 2025/12
Y1 - 2025/12
N2 - Recent molecular generation models for structure-based drug design (SBDD) often produce unrealistic 3D molecules due to the neglect of structural feasibility and drug-like properties. In this paper, we introduce DiffGui, a target-conditioned E(3)-equivariant diffusion model that integrates bond diffusion and property guidance, to address the above challenges. The combination of atom diffusion and bond diffusion guarantees the concurrent generation of both atoms and bonds by explicitly modeling their interdependencies. Property guidance incorporates the binding affinity and drug-like properties of molecules into the training and sampling processes. Extensive experiments prove that DiffGui outperforms existing methods in generating molecules with high binding affinity, rational chemical structure, and desirable properties. Ablation studies confirm the importance of bond diffusion and property guidance modules. DiffGui demonstrates effectiveness in both de novo drug design and lead optimization, with validation through wet-lab experiments.
AB - Recent molecular generation models for structure-based drug design (SBDD) often produce unrealistic 3D molecules due to the neglect of structural feasibility and drug-like properties. In this paper, we introduce DiffGui, a target-conditioned E(3)-equivariant diffusion model that integrates bond diffusion and property guidance, to address the above challenges. The combination of atom diffusion and bond diffusion guarantees the concurrent generation of both atoms and bonds by explicitly modeling their interdependencies. Property guidance incorporates the binding affinity and drug-like properties of molecules into the training and sampling processes. Extensive experiments prove that DiffGui outperforms existing methods in generating molecules with high binding affinity, rational chemical structure, and desirable properties. Ablation studies confirm the importance of bond diffusion and property guidance modules. DiffGui demonstrates effectiveness in both de novo drug design and lead optimization, with validation through wet-lab experiments.
UR - https://www.scopus.com/pages/publications/105014627297
U2 - 10.1038/s41467-025-63245-0
DO - 10.1038/s41467-025-63245-0
M3 - 文章
AN - SCOPUS:105014627297
SN - 2041-1723
VL - 16
JO - Nature Communications
JF - Nature Communications
IS - 1
M1 - 7928
ER -