对比几何学习实现统一的结构与配体药物设计
Contrastive Geometric Learning Unlocks Unified Structure- and Ligand-Based Drug Design
AI总结：
提出对比几何模型ConGLUDe，统一结构与配体训练，实现虚拟筛选、靶标钓鱼和配体条件口袋预测，在多项基准测试中表现优异。
摘要：
基于结构和基于配体的计算药物设计传统上依赖于不相关的数据源和建模假设，限制了它们在大规模上的联合使用。在这项工作中，我们引入了用于统一计算药物设计的对比几何学习（ConGLUDe），这是一个单一的对比几何模型，统一了基于结构和基于配体的训练。ConGLUDe将产生全蛋白质表示和预测结合位点的隐式嵌入的几何蛋白质编码器与快速配体编码器耦合，消除了对预定义口袋的需求。通过对比学习将配体与全局蛋白质表示和多个候选结合位点对齐，ConGLUDe除了支持虚拟筛选和靶标钓鱼外，还支持配体条件口袋预测，同时在蛋白质-配体复合物和大规模生物活性数据上联合训练。在多种基准测试中，ConGLUDe实现了具有竞争力的零样本虚拟筛选性能，在具有挑战性的靶标钓鱼任务上显著优于现有方法，并展示了最先进的配体条件口袋选择。这些结果突显了统一结构-配体训练的优势，并将ConGLUDe定位为迈向药物发现通用基础模型的一步。
英文摘要：
Structure-based and ligand-based computational drug design have traditionally relied on disjoint data sources and modeling assumptions, limiting their joint use at scale. In this work, we introduce Contrastive Geometric Learning for Unified Computational Drug Design (ConGLUDe), a single contrastive geometric model that unifies structure- and ligand-based training. ConGLUDe couples a geometric protein encoder that produces whole-protein representations and implicit embeddings of predicted binding sites with a fast ligand encoder, removing the need for predefined pockets. By aligning ligands with both global protein representations and multiple candidate binding sites through contrastive learning, ConGLUDe supports ligand-conditioned pocket prediction in addition to virtual screening and target fishing, while being trained jointly on protein-ligand complexes and large-scale bioactivity data. Across diverse benchmarks, ConGLUDe achieves competitive zero-shot virtual screening performance, substantially outperforms existing methods on a challenging target fishing task, and demonstrates state-of-the-art ligand-conditioned pocket selection. These results highlight the advantages of unified structure-ligand training and position ConGLUDe as a step toward general-purpose foundation models for drug discovery.
机构、总结、中文摘要均由AI分析而来，可能存在错误，请以论文正文为准。
