HiGraphDTI: Hierarchical Graph Representation Learning for Drug-Target Interaction Prediction
- URL: http://arxiv.org/abs/2404.10561v1
- Date: Tue, 16 Apr 2024 13:35:24 GMT
- Title: HiGraphDTI: Hierarchical Graph Representation Learning for Drug-Target Interaction Prediction
- Authors: Bin Liu, Siqi Wu, Jin Wang, Xin Deng, Ao Zhou,
- Abstract summary: We propose a hierarchical graph representation learning-based DTI prediction method (HiGraphDTI)
Specifically, HiGraphDTI learns hierarchical drug representations from triple-level molecular graphs to thoroughly exploit chemical information embedded in atoms, motifs, and molecules.
An attentional feature fusion module incorporates information from different receptive fields to extract expressive target features.
- Score: 15.005837084219355
- License: http://arxiv.org/licenses/nonexclusive-distrib/1.0/
- Abstract: The discovery of drug-target interactions (DTIs) plays a crucial role in pharmaceutical development. The deep learning model achieves more accurate results in DTI prediction due to its ability to extract robust and expressive features from drug and target chemical structures. However, existing deep learning methods typically generate drug features via aggregating molecular atom representations, ignoring the chemical properties carried by motifs, i.e., substructures of the molecular graph. The atom-drug double-level molecular representation learning can not fully exploit structure information and fails to interpret the DTI mechanism from the motif perspective. In addition, sequential model-based target feature extraction either fuses limited contextual information or requires expensive computational resources. To tackle the above issues, we propose a hierarchical graph representation learning-based DTI prediction method (HiGraphDTI). Specifically, HiGraphDTI learns hierarchical drug representations from triple-level molecular graphs to thoroughly exploit chemical information embedded in atoms, motifs, and molecules. Then, an attentional feature fusion module incorporates information from different receptive fields to extract expressive target features.Last, the hierarchical attention mechanism identifies crucial molecular segments, which offers complementary views for interpreting interaction mechanisms. The experiment results not only demonstrate the superiority of HiGraphDTI to the state-of-the-art methods, but also confirm the practical ability of our model in interaction interpretation and new DTI discovery.
Related papers
- FARM: Functional Group-Aware Representations for Small Molecules [55.281754551202326]
We introduce Functional Group-Aware Representations for Small Molecules (FARM)
FARM is a foundation model designed to bridge the gap between SMILES, natural language, and molecular graphs.
We rigorously evaluate FARM on the MoleculeNet dataset, where it achieves state-of-the-art performance on 10 out of 12 tasks.
arXiv Detail & Related papers (2024-10-02T23:04:58Z) - Contrastive Dual-Interaction Graph Neural Network for Molecular Property Prediction [0.0]
We introduce DIG-Mol, a novel self-supervised graph neural network framework for molecular property prediction.
DIG-Mol integrates a momentum distillation network with two interconnected networks to efficiently improve molecular characterization.
We have established DIG-Mol's state-of-the-art performance through extensive experimental evaluation in a variety of molecular property prediction tasks.
arXiv Detail & Related papers (2024-05-04T10:09:27Z) - MolGrapher: Graph-based Visual Recognition of Chemical Structures [50.13749978547401]
We introduce MolGrapher to recognize chemical structures visually.
We treat all candidate atoms and bonds as nodes and put them in a graph.
We classify atom and bond nodes in the graph with a Graph Neural Network.
arXiv Detail & Related papers (2023-08-23T16:16:11Z) - GraphCL-DTA: a graph contrastive learning with molecular semantics for
drug-target binding affinity prediction [2.523552067304274]
GraphCL-DTA is a graph contrastive learning framework for molecular graphs to learn drug representations.
Next, we design a new loss function that can be directly used to adjust the uniformity of drug and target representations.
The effectiveness of the above innovative elements is verified on two real datasets.
arXiv Detail & Related papers (2023-07-18T06:01:37Z) - Bi-level Contrastive Learning for Knowledge-Enhanced Molecule
Representations [55.42602325017405]
We propose a novel method called GODE, which takes into account the two-level structure of individual molecules.
By pre-training two graph neural networks (GNNs) on different graph structures, combined with contrastive learning, GODE fuses molecular structures with their corresponding knowledge graph substructures.
When fine-tuned across 11 chemical property tasks, our model outperforms existing benchmarks, registering an average ROC-AUC uplift of 13.8% for classification tasks and an average RMSE/MAE enhancement of 35.1% for regression tasks.
arXiv Detail & Related papers (2023-06-02T15:49:45Z) - Atomic and Subgraph-aware Bilateral Aggregation for Molecular
Representation Learning [57.670845619155195]
We introduce a new model for molecular representation learning called the Atomic and Subgraph-aware Bilateral Aggregation (ASBA)
ASBA addresses the limitations of previous atom-wise and subgraph-wise models by incorporating both types of information.
Our method offers a more comprehensive way to learn representations for molecular property prediction and has broad potential in drug and material discovery applications.
arXiv Detail & Related papers (2023-05-22T00:56:00Z) - HiGNN: Hierarchical Informative Graph Neural Networks for Molecular
Property Prediction Equipped with Feature-Wise Attention [5.735627221409312]
We propose a well-designed hierarchical informative graph neural networks framework (termed HiGNN) for predicting molecular property.
Experiments demonstrate that HiGNN achieves state-of-the-art predictive performance on many challenging drug discovery-associated benchmark datasets.
arXiv Detail & Related papers (2022-08-30T05:16:15Z) - Graph neural networks for the prediction of molecular structure-property
relationships [59.11160990637615]
Graph neural networks (GNNs) are a novel machine learning method that directly work on the molecular graph.
GNNs allow to learn properties in an end-to-end fashion, thereby avoiding the need for informative descriptors.
We describe the fundamentals of GNNs and demonstrate the application of GNNs via two examples for molecular property prediction.
arXiv Detail & Related papers (2022-07-25T11:30:44Z) - Hierarchical Graph Representation Learning for the Prediction of
Drug-Target Binding Affinity [7.023929372010717]
We propose a novel hierarchical graph representation learning model for the drug-target binding affinity prediction, namely HGRL-DTA.
In this paper, we adopt a message broadcasting mechanism to integrate the hierarchical representations learned from the global-level affinity graph and the local-level molecular graph. Besides, we design a similarity-based embedding map to solve the cold start problem of inferring representations for unseen drugs and targets.
arXiv Detail & Related papers (2022-03-22T04:50:16Z) - Drug-Target Interaction Prediction with Graph Attention networks [26.40249934284416]
We present an end-to-end framework, DTI-GAT (Drug-Target Interaction prediction with Graph Attention networks) for DTI predictions.
DTI-GAT incorporates a deep network neural architecture that operates on graph-structured data with the attention mechanism.
Experimental evaluations show that DTI-GAT outperforms various state-of-the-art systems on the binary DTI prediction problem.
arXiv Detail & Related papers (2021-07-10T07:06:36Z) - MolTrans: Molecular Interaction Transformer for Drug Target Interaction
Prediction [68.5766865583049]
Drug target interaction (DTI) prediction is a foundational task for in silico drug discovery.
Recent years have witnessed promising progress for deep learning in DTI predictions.
We propose a Molecular Interaction Transformer (TransMol) to address these limitations.
arXiv Detail & Related papers (2020-04-23T18:56:04Z)
This list is automatically generated from the titles and abstracts of the papers in this site.
This site does not guarantee the quality of this site (including all information) and is not responsible for any consequences.