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DiffDec: Structure-Aware Scaffold Decoration with an End-to-End Diffusion Model

脚手架 二面角 化学 对接(动物) 分子 分子动力学 计算机科学 群(周期表) 生物系统 计算化学 氢键 生物 数据库 医学 护理部 有机化学
作者
Junjie Xie,Sheng Chen,Jinping Lei,Yuedong Yang
出处
期刊:Journal of Chemical Information and Modeling [American Chemical Society]
卷期号:64 (7): 2554-2564 被引量:25
标识
DOI:10.1021/acs.jcim.3c01466
摘要

In molecular optimization, one popular way is R-group decoration on molecular scaffolds, and many efforts have been made to generate R-groups based on deep generative models. However, these methods mostly use information on known binding ligands, without fully utilizing target structure information. In this study, we proposed a new method, DiffDec, to involve 3D pocket constraints by a modified diffusion technique for optimizing molecules through molecular scaffold decoration. For end-to-end generation of R-groups with different sizes, we designed a novel fake atom mechanism. DiffDec was shown to be able to generate structure-aware R-groups with realistic geometric substructures by the analysis of bond angles and dihedral angles and simultaneously generate multiple R-groups for one scaffold on different growth anchors. The growth anchors could be provided by users or automatically determined by our model. DiffDec achieved R-group recovery rates of 69.67% and 45.34% in the single and multiple R-group decoration tasks, respectively, and these values were significantly higher than competing methods (37.33% and 26.85%). According to the molecular docking study, our decorated molecules obtained a better average binding affinity than baseline methods. The docking pose analysis revealed that DiffDec could decorate scaffolds with R-groups that exhibited improved binding affinities and more favorable interactions with the pocket. These results demonstrated the potential and applicability of DiffDec in real-world scaffold decoration for molecular optimization.
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