TSMGen: Target-Specific Molecule Generation via Higher-Order Structural Dependencies and Context-Aware Bidirectional Fusion
Yaoyu Chen, Xiaoli Lin, Ziyi Gong, Jun Pang
ICML 2026 regular
Tóm tắt (nguồn: OpenReview · © tác giả)
Efficiently designing high-quality molecules targeting disease-relevant targets is a critical challenge. Most existing methods can capture pairwise amino acid relations, neglecting the higher-order relations among multiple amino acids. This paper proposes a target-specific molecule generation framework, namely TSMGen, to comprehensively capture the local and global structural information of the protein pocket by modeling higher-order spatial dependencies both at the atomic and the amino acid levels. Furthermore, we design a context-aware bidirectional fusion module to learn the more detailed structural information about the protein pocket. This module simultaneously attends to features from both the protein pocket and the molecule, fully leveraging the structural information from both to optimize the generation process of targeted molecules, thereby enhancing the quality of generated molecules. Experiments show that TSMGen outperforms state-of-the-art methods in terms of Vina Score, High Affinity, QED, SA and Diversity, and a case study on $\beta$-secretase enzyme further confirms its ability to generate molecules with stronger binding affinity.
Từ khoá
Metadata từ BioTender-max/icml2026-ai-bio (CC0-1.0). Phở không lưu trữ bản PDF; link trỏ về nguồn gốc.
Cùng chủ đề
Towards Sub-Second Molecular Docking as a Structural Primitive: A Quantized Consistency Diffusion Framework
Kexin Zhang, Weichen Qin, Yue Teng, Jiale Yu +4
Agent-centered scientific discovery is turning scientific models into always-on computational infrastructure. In this paradigm, AI agents coordinate tools, interpret feedback, and…
A Call to Lagrangian Action: Learning Population Mechanics from Temporal Snapshots
Vincent Guan, Lazar Atanackovic, Kirill Neklyudov
The population dynamics of molecules, cells, and organisms are governed by a number of unknown internal and external forces. In the last decade, population dynamics have…
DeCoDe: Decoupling Binding Position and Molecular Conformation in 3D Ligand Diffusion for Structure-Based Drug Design
Julong Yang, Wen Huang, Junhui Chen, Jian Peng
Recent advances in diffusion models show promise for Structure-Based Drug Design (SBDD), which aims to generate 3D ligand molecules that bind tightly to specific protein targets.…