灵活性(工程)
配体(生物化学)
分子
化学
小分子
蛋白质配体
生物系统
蛋白质结构
限制
计算机科学
血浆蛋白结合
生物物理学
扩散
生成模型
药物发现
生成语法
计算生物学
分子动力学
化学物理
蛋白质设计
蛋白质动力学
分子生物物理学
构象集合
蛋白质折叠
蛋白质-蛋白质相互作用
蛋白质工程
结合位点
结晶学
作者
Xinzhe Zheng,Shiyu Jiang,Gustavo de Miranda Seabra,Chenglong Li,Yanjun Li
标识
DOI:10.1609/aaai.v40i2.37138
摘要
Deep generative models are rapidly advancing structure-based drug design, offering substantial promise for generating small molecule ligands that bind to specific protein targets. However, most current approaches assume a rigid protein binding pocket, neglecting the intrinsic flexibility of proteins and the conformational rearrangements induced by ligand binding, limiting their applicability in practical drug discovery. Here, we propose Apo2Mol, a diffusion-based generative framework for 3D molecule design that explicitly accounts for conformational flexibility in protein binding pockets. To support this, we curate a dataset of over 24,000 experimentally resolved apo-holo structure pairs from the Protein Data Bank, enabling the characterization of protein structure changes associated with ligand binding. Apo2Mol employs a full-atom hierarchical graph-based diffusion model that simultaneously generates 3D ligand molecules and their corresponding holo pocket conformations from input apo states. Empirical studies demonstrate that Apo2Mol can achieve state-of-the-art performance in generating high-affinity ligands and accurately capture realistic protein pocket conformational changes.
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