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

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.

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Journal
Journal of Chemical Information and Modeling
Published
2026-10-07
DOI
https://doi.org/10.1021/acs.jcim.6c02487
Primary Topic
Computational Drug Discovery Methods
Type
article
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article

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

Xiao Dong He, Jinrong Yang, Baochuan Hu, Dongliang Chen et al.
Journal of Chemical Information and Modeling
Computational Drug Discovery Methods
article

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

Xiao Dong He, Jinrong Yang, Baochuan Hu, Dongliang Chen, Xiushan Wu
article en

Abstract

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.

Journal of Chemical Information and Modeling
New York University Shanghai (CN), Anqing Normal University (CN), East China Normal University (CN)
Openalex Percentile: Top 13%
Computational Drug Discovery Methods
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