ArticleCommunications biology2024
Annotating protein functions via fusing multiple biological modalities.
Article in Communications biology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.
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Who cites it
9 citing papers in PubMed.
- A Novel Cancer Driver Genes Identification Method Based on Self-Supervised Dual Masked Graph Autoencoder.Interdisciplinary sciences, computational life sciences · 2026Article
- Dynamics-informed multigraph neural networks for protein thermostability prediction and residue-level interpretation.iScience · 2026Article
- ProSSF: integrating sequence, structure, and gene ontology for prediction of protein stability, interaction, and function.Molecular genetics and genomics : MGG · 2026Article
- IQSPred-PLM: An Interpretable Quorum Sensing Peptides Prediction Model Based on Protein Language Model.Interdisciplinary sciences, computational life sciences · 2026Article
- Artificial intelligence-enabled multi-scale virtual cell: perspective, challenges, and opportunities.Briefings in bioinformatics · 2026Review
- Structure-sensitive transformer and multi-view graph contrastive learning enhanced prediction of drug-related microbes.BMC bioinformatics · 2025Article
- SuperEdgeGO: Edge-supervised graph representation learning for enhanced protein function prediction.PLoS computational biology · 2025Article
- GOBeacon: An ensemble model for protein function prediction enhanced by contrastive learning.Protein science : a publication of the Protein Society · 2025Article
- MSNGO: multi-species protein function annotation based on 3D protein structure and network propagation.Bioinformatics (Oxford, England) · 2025Article
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Authors and funding
5 authors.
Funding
Abstract
Understanding the function of proteins is of great significance for revealing disease pathogenesis and discovering new targets. Benefiting from the explosive growth of the protein universal, deep learning has been applied to accelerate the protein annotation cycle from different biological modalities. However, most existing deep learning-based methods not only fail to effectively fuse different biological modalities, resulting in low-quality protein representations, but also suffer from the convergence of suboptimal solution caused by sparse label representations. Aiming at the above issue, we propose a multiprocedural approach for fusing heterogeneous biological modalities and annotating protein functions, i.e., MIF2GO (Multimodal Information Fusion to infer Gene Ontology terms), which sequentially fuses up to six biological modalities ranging from different biological levels in three steps, thus leading to powerful protein representations. Evaluation results on seven benchmark datasets show that the proposed method not only considerably outperforms state-of-the-art performance, but also demonstrates great robustness and generalizability across species. Besides, we also present biological insights into the associations between those modalities and protein functions. This research provides a robust framework for integrating multimodal biological data, offering a scalable solution for protein function annotation, ultimately facilitating advancements in precision medicine and the discovery of novel therapeutic strategies.
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Registered trials
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