Hierarchical graph transformer with contrastive learning for protein function prediction

• Published in: Bioinformatics (Oxford, England) Vol. 39; no. 7
• Main Authors: Gu, Zhonghui, Luo, Xiao, Chen, Jiaxiao, Deng, Minghua, Lai, Luhua
• Format: Journal Article
• Language: English
• Published: England Oxford University Press 01.07.2023
• Subjects: Amino Acid Sequence; Benchmarking; High-Throughput Nucleotide Sequencing; Neural Networks, Computer; Original Paper; Semantics
• ISSN: 1367-4811; 1367-4803; 1367-4811
• DOI: 10.1093/bioinformatics/btad410

Abstract Motivation In recent years, high-throughput sequencing technologies have made large-scale protein sequences accessible. However, their functional annotations usually rely on low-throughput and pricey experimental studies. Computational prediction models offer a promising alternative to accelerate this process. Graph neural networks have shown significant progress in protein research, but capturing long-distance structural correlations and identifying key residues in protein graphs remains challenging. Results In the present study, we propose a novel deep learning model named Hierarchical graph transformEr with contrAstive Learning (HEAL) for protein function prediction. The core feature of HEAL is its ability to capture structural semantics using a hierarchical graph Transformer, which introduces a range of super-nodes mimicking functional motifs to interact with nodes in the protein graph. These semantic-aware super-node embeddings are then aggregated with varying emphasis to produce a graph representation. To optimize the network, we utilized graph contrastive learning as a regularization technique to maximize the similarity between different views of the graph representation. Evaluation of the PDBch test set shows that HEAL-PDB, trained on fewer data, achieves comparable performance to the recent state-of-the-art methods, such as DeepFRI. Moreover, HEAL, with the added benefit of unresolved protein structures predicted by AlphaFold2, outperforms DeepFRI by a significant margin on Fmax, AUPR, and Smin metrics on PDBch test set. Additionally, when there are no experimentally resolved structures available for the proteins of interest, HEAL can still achieve better performance on AFch test set than DeepFRI and DeepGOPlus by taking advantage of AlphaFold2 predicted structures. Finally, HEAL is capable of finding functional sites through class activation mapping. Availability and implementation Implementations of our HEAL can be found at https://github.com/ZhonghuiGu/HEAL.