Unified Multitask Model for Aquatic Toxicity Prediction across Organism Groups and Effect End Points: A Comparison of Molecular Representations

IF 6.4 2区 化学 Q1 CHEMISTRY, MEDICINAL
Xiushan Wu, Baochuan Hu, Dongliang Chen, Jinrong Yang, Xiao He
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引用次数: 0

Abstract

Computational prediction of aquatic toxicity provides a rapid and cost-efficient alternative to resource-intensive in vivo ecotoxicological testing. However, most existing models adopt a fragmented modeling strategy, developing separate models for each organism group and toxicity end point. Such task-specific models restrict knowledge transfer across related biological contexts and fail to account for the biological ordering between multiple effect concentrations (EC50/EC10). Here, we propose a unified multitask framework to simultaneously predict effect concentrations for three aquatic organism groups (fish, crustaceans, algae) and two end points (EC50/EC10) within a single model. This framework integrates a molecular encoder with a Multigate Mixture-of-Experts (MMoE) network, a soft end point-ordering term that encourages the biological relation EC50 ≥ EC10, and a heteroscedastic regression output that provides per-prediction uncertainty estimates. We evaluated a multirepresentation fusion encoder combining physicochemical descriptors, molecular fingerprints, and a 2D molecular graph neural network (GNN), together with 3D-pretrained Uni-Mol and TRIDENT baselines. Under a common global scaffold/acyclic-cluster 5-fold pooled out-of-fold (OOF) protocol, the multirepresentation fusion model demonstrated robust predictive performance across all six organism–end point tasks, with lower prediction errors than TRIDENT across all six tasks and Uni-Mol in four tasks. Attention-based interpretation further highlighted chemically meaningful atoms and substructures that were consistent with plausible toxicity-relevant structural motifs. Together, these findings demonstrate that integrating multitask learning, biologically informed end point constraints, and complementary molecular representations provides a promising foundation for broadly applicable and uncertainty-aware models of aquatic toxicity.

跨生物群体和效应终点的水生毒性预测的统一多任务模型:分子表征的比较
水生毒性的计算预测为资源密集的体内生态毒理学测试提供了一种快速而经济的替代方法。然而,大多数现有模型采用碎片化建模策略,为每个生物群体和毒性终点开发单独的模型。这种任务特定模型限制了相关生物学背景下的知识转移,并且无法解释多种效应浓度之间的生物顺序(EC50/EC10)。在此,我们提出了一个统一的多任务框架来同时预测三个水生生物群体(鱼类、甲壳类、藻类)和两个终点(EC50/EC10)在一个单一模型中的效应浓度。该框架集成了一个带有多门混合专家(MMoE)网络的分子编码器,一个鼓励生物关系EC50≥EC10的软端点排序项,以及一个提供预预测不确定性估计的异方差回归输出。我们评估了一种多表示融合编码器,该编码器结合了物理化学描述符、分子指纹、2D分子图神经网络(GNN)以及3d预训练的Uni-Mol和TRIDENT基线。在通用的全局支架/无环簇5-fold pooled out- fold (OOF)协议下,多表示融合模型在所有6个生物体端点任务中表现出稳健的预测性能,在所有6个任务中的预测误差低于TRIDENT,在4个任务中的预测误差低于Uni-Mol。基于注意力的解释进一步强调了化学上有意义的原子和亚结构,这些原子和亚结构与可能的毒性相关结构基序一致。总之,这些发现表明,整合多任务学习、生物学信息终点约束和互补的分子表征为广泛适用和不确定性感知的水生毒性模型提供了有希望的基础。
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来源期刊
CiteScore
9.80
自引率
10.70%
发文量
529
审稿时长
1.4 months
期刊介绍: The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery. Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field. As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.
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