HeMeNet: Heterogeneous Multichannel Equivariant Network for Protein Multi-task Learning

Understanding and leveraging the 3D structures of proteins is central to a variety of biological and drug discovery tasks. While deep learning has been applied successfully for structure-based protein function prediction tasks, current methods usually employ distinct training for each task. However, each of the tasks is of small size, and such a single-task strategy hinders the models' performance and generalization ability. As some labeled 3D protein datasets are biologically related, combining multi-source datasets for larger-scale multi-task learning is one way to overcome this problem. In this paper, we propose a neural network model to address multiple tasks jointly upon the input of 3D protein structures. In particular, we first construct a standard structure-based multi-task benchmark called Protein-MT, consisting of 6 biologically relevant tasks, including affinity prediction and property prediction, integrated from 4 public datasets. Then, we develop a novel graph neural network for multi-task learning, dubbed Heterogeneous Multichannel Equivariant Network (HeMeNet), which is E(3) equivariant and able to capture heterogeneous relationships between different atoms. Besides, HeMeNet can achieve task-specific learning via the task-aware readout mechanism. Extensive evaluations of our benchmark verify the effectiveness of multi-task learning, and our model generally surpasses state-of-the-art models.

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Publication Details

Journal
Proceedings of the AAAI Conference on Artificial Intelligence
Published
2025-04-11
DOI
https://doi.org/10.1609/aaai.v39i1.32000
Citations
1
Primary Topic
Machine Learning in Bioinformatics
Type
article
Field-Weighted Citation Impact
2.07

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article

HeMeNet: Heterogeneous Multichannel Equivariant Network for Protein Multi-task Learning

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1 citations
Proceedings of the AAAI Conference on Artificial Intelligence
Machine Learning in Bioinformatics
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article

HeMeNet: Heterogeneous Multichannel Equivariant Network for Protein Multi-task Learning

Zhiqiang Zhang, Wenbing Huang, Jiaming Shen, Jun Zhou, Ting Chen, Rong Han, Lingxiao Luo, Xinyan Han
article en
1 citations

Abstract

Understanding and leveraging the 3D structures of proteins is central to a variety of biological and drug discovery tasks. While deep learning has been applied successfully for structure-based protein function prediction tasks, current methods usually employ distinct training for each task. However, each of the tasks is of small size, and such a single-task strategy hinders the models' performance and generalization ability. As some labeled 3D protein datasets are biologically related, combining multi-source datasets for larger-scale multi-task learning is one way to overcome this problem. In this paper, we propose a neural network model to address multiple tasks jointly upon the input of 3D protein structures. In particular, we first construct a standard structure-based multi-task benchmark called Protein-MT, consisting of 6 biologically relevant tasks, including affinity prediction and property prediction, integrated from 4 public datasets. Then, we develop a novel graph neural network for multi-task learning, dubbed Heterogeneous Multichannel Equivariant Network (HeMeNet), which is E(3) equivariant and able to capture heterogeneous relationships between different atoms. Besides, HeMeNet can achieve task-specific learning via the task-aware readout mechanism. Extensive evaluations of our benchmark verify the effectiveness of multi-task learning, and our model generally surpasses state-of-the-art models.

Proceedings of the AAAI Conference on Artificial IntelligenceVol. 39(1)
Renmin University of China (CN), Tsinghua University (CN)
Ant Group, National Natural Science Foundation of China, Tsinghua University, Renmin University of China, Beijing National Research Center For Information Science And Technology, Beijing Nova Program, Fundamental Research Funds for the Central Universities
Openalex Percentile: Top 14%
Machine Learning in Bioinformatics
2.07
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