计算机科学
深度学习
人工智能
互补性(分子生物学)
深层神经网络
药物发现
分子识别
第一代
分子结合
机器学习
纳米技术
人工神经网络
分子动力学
分子描述符
合成数据
分子模型
分子工程
分子构象
训练集
作者
Taojie Kuang,Qianli Ma,Athanasios V. Vasilakos,Yu Wang,Qiang (Shawn) Cheng,Zhixiang Ren
摘要
In recent years, deep learning techniques have made significant strides in molecular generation for specific targets, driving advancements in drug discovery. However, existing molecular generation methods present significant limitations: those operating at the atomic level often lack synthetic feasibility, drug-likeness, and interpretability, while fragment-based approaches frequently overlook comprehensive factors that influence protein–molecule interactions. To address these challenges, we propose a novel fragment-based molecular generation framework tailored for specific proteins. Our method begins by constructing a protein subpocket and molecular arm concept-based neural network, which systematically integrates interaction force information and geometric complementarity to sample molecular arms for specific protein subpockets. Subsequently, we introduce a diffusion model to generate molecular backbones that connect these arms, ensuring structural integrity and chemical diversity. Our approach improves synthetic feasibility and binding affinity, with a 4% increase in drug-likeness and a 6% improvement in synthetic feasibility. Furthermore, by integrating explicit interaction data through a concept-based model, our framework enhances interpretability, offering valuable insights into the molecular design process.
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