药物发现
计算机科学
催交
数据集成
计算生物学
桥接(联网)
图形
药物重新定位
机器学习
人工智能
药品
数据挖掘
生物信息学
生物
理论计算机科学
工程类
计算机网络
系统工程
药理学
作者
Qing Ye,Yundian Zeng,Lei Jiang,Yu Kang,Peichen Pan,Jiming Chen,Yafeng Deng,Haitao Zhao,Shibo He,Tingjun Hou,Chang‐Yu Hsieh
标识
DOI:10.1002/advs.202412402
摘要
Discovering therapeutic molecules requires the integration of both phenotype-based drug discovery (PDD) and target-based drug discovery (TDD). However, this integration remains challenging due to the inherent heterogeneity, noise, and bias present in biomedical data. In this study, Knowledge-Guided Drug Relational Predictor (KGDRP), a graph representation learning approach is developed that effectively integrates multimodal biomedical data, including network data containing biological system information, gene expression data, and sequence data that incorporates chemical molecular structures, all within a heterogeneous graph (HG) structure. By incorporating biomedical HG (BioHG) into a heterogeneous graph neural network (HGNN)-based architecture, KGDRP exhibits a remarkable 12% improvement compared to previous methods in real-world screening scenarios. Notably, the biology-informed representation, derived from KGDRP, significantly enhance target prioritization by 26% in drug target discovery. Furthermore, zero-shot evaluation on COVID-19 exhibited a notably higher success rate in identifying diverse potential drugs. The utilization of BioHG facilitates a unique KGDRP-based analysis of cell-target-drug interactions, thereby enabling the elucidation of drug mechanisms. Overall, KGDRP provides a robust infrastructure for the seamlessly integration of multimodal data and biomedical networks, effectively accelerating PDD, guiding therapeutic target discovery, and ultimately expediting therapeutic molecule discovery.
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