可解释性
计算机科学
概化理论
鉴定(生物学)
代表(政治)
机器学习
数量结构-活动关系
毒性
计算生物学
生化工程
人工智能
人类健康
危害
方案(数学)
肝毒性
风险分析(工程)
计算模型
虚拟筛选
数据挖掘
生物系统
化学
风险评估
化学毒性
优先次序
危害分析
水生毒理学
药物毒性
作者
Lianlian Wu,Fanmeng Wang,Yixin Zhang,Ruijiang Li,Yanpeng Zhao,Hongteng Xu,Zhifeng Gao,Song He,Xiaochen Bo
标识
DOI:10.1021/acs.est.5c04614
摘要
Hazard identification and labeling of industrial chemicals and their released environmental pollutants are crucial for mitigating ecological and health risks. Comprehensive evaluation of multiple toxicity end points is essential to fully characterize chemical hazards. Existing deep-learning-based toxicity prediction models often exhibit poor generalizability, especially for rare toxicities with sparse data. Most studies fail to capture the three-dimensional (3D) spatial arrangement and stereochemical properties of chemicals, as well as the interrelated nature among end points, hindering accurate toxicity profiling. Here, we propose ToxScan, an SE(3)-equivariant multiscale model, as a universal toxicity prediction framework to address these issues. It incorporates 3D geometry information through a two-level molecular and atomic representation learning protocol. A parallel multiscale modeling and a multitask learning scheme are applied to learn universal toxicological characteristics. Results show that ToxScan achieves 7.8-37.6% improvements over state-of-the-art models for medium-/small-scale end points, demonstrates differentiation of structural analogues with contrasting toxicities, and maintains generalizability to environmental pollutants. Interpretability analysis at the atomic and molecular levels reveals identifiable atomic interaction patterns and potential structural alerts. Case studies reveal its capacity to detect subtle structural determinants while elucidating the mechanisms of pollutants. To facilitate user accessibility, we provide an intuitive web platform (https://funmg.dp.tech/Toxscan) for the rapid prediction of multiple toxicity end points of new compounds.
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