{"title":"NASNet-DTI:利用异构图和节点自适应准确预测药物-靶标相互作用。","authors":"Ningyu Zhong, Zhihua Du","doi":"10.1093/bib/bbaf342","DOIUrl":null,"url":null,"abstract":"<p><p>Drug-target interactions (DTIs) play a key role in drug development, and accurate prediction can significantly improve the efficiency of this process. Traditional experimental methods are reliable but time-consuming and laborious. With the rapid development of deep learning, many DTI prediction methods have emerged. However, most of these methods only focus on the intrinsic features of drugs and targets, while ignoring the relational features between them. In addition, existing graph-based DTI prediction methods often face the challenge of over-smoothing in graph neural networks (GNNs), which limits their prediction accuracy. To address these issues, we propose NASNet-DTI (Drug-target Interactions Based on Node Adaptation and Similarity Networks), a new framework designed to overcome these limitations. NASNet-DTI uses graph convolutional network to extract features from drug molecules and targets separately, and constructs heterogeneous networks to represent two types of nodes: drugs and targets. The edges in the network describe their multiple relationships: drug-drug, target-target, and drug-target. In the feature learning stage, NASNet-DTI adopts a node adaptive learning strategy to dynamically determine the optimal aggregation depth for each node. This ensures that each node can learn the most discriminative features, which effectively alleviates the over-smoothing problem and improves prediction accuracy. Experimental results show that NASNet-DTI significantly outperforms existing methods on multiple datasets, demonstrating its effectiveness and potential as a powerful tool to advance drug discovery and development.</p>","PeriodicalId":9209,"journal":{"name":"Briefings in bioinformatics","volume":"26 4","pages":""},"PeriodicalIF":7.7000,"publicationDate":"2025-07-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12265895/pdf/","citationCount":"0","resultStr":"{\"title\":\"NASNet-DTI: accurate drug-target interaction prediction using heterogeneous graphs and node adaptation.\",\"authors\":\"Ningyu Zhong, Zhihua Du\",\"doi\":\"10.1093/bib/bbaf342\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Drug-target interactions (DTIs) play a key role in drug development, and accurate prediction can significantly improve the efficiency of this process. Traditional experimental methods are reliable but time-consuming and laborious. With the rapid development of deep learning, many DTI prediction methods have emerged. However, most of these methods only focus on the intrinsic features of drugs and targets, while ignoring the relational features between them. In addition, existing graph-based DTI prediction methods often face the challenge of over-smoothing in graph neural networks (GNNs), which limits their prediction accuracy. To address these issues, we propose NASNet-DTI (Drug-target Interactions Based on Node Adaptation and Similarity Networks), a new framework designed to overcome these limitations. NASNet-DTI uses graph convolutional network to extract features from drug molecules and targets separately, and constructs heterogeneous networks to represent two types of nodes: drugs and targets. The edges in the network describe their multiple relationships: drug-drug, target-target, and drug-target. In the feature learning stage, NASNet-DTI adopts a node adaptive learning strategy to dynamically determine the optimal aggregation depth for each node. This ensures that each node can learn the most discriminative features, which effectively alleviates the over-smoothing problem and improves prediction accuracy. Experimental results show that NASNet-DTI significantly outperforms existing methods on multiple datasets, demonstrating its effectiveness and potential as a powerful tool to advance drug discovery and development.</p>\",\"PeriodicalId\":9209,\"journal\":{\"name\":\"Briefings in bioinformatics\",\"volume\":\"26 4\",\"pages\":\"\"},\"PeriodicalIF\":7.7000,\"publicationDate\":\"2025-07-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12265895/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Briefings in bioinformatics\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1093/bib/bbaf342\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"BIOCHEMICAL RESEARCH METHODS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Briefings in bioinformatics","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1093/bib/bbaf342","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"BIOCHEMICAL RESEARCH METHODS","Score":null,"Total":0}
NASNet-DTI: accurate drug-target interaction prediction using heterogeneous graphs and node adaptation.
Drug-target interactions (DTIs) play a key role in drug development, and accurate prediction can significantly improve the efficiency of this process. Traditional experimental methods are reliable but time-consuming and laborious. With the rapid development of deep learning, many DTI prediction methods have emerged. However, most of these methods only focus on the intrinsic features of drugs and targets, while ignoring the relational features between them. In addition, existing graph-based DTI prediction methods often face the challenge of over-smoothing in graph neural networks (GNNs), which limits their prediction accuracy. To address these issues, we propose NASNet-DTI (Drug-target Interactions Based on Node Adaptation and Similarity Networks), a new framework designed to overcome these limitations. NASNet-DTI uses graph convolutional network to extract features from drug molecules and targets separately, and constructs heterogeneous networks to represent two types of nodes: drugs and targets. The edges in the network describe their multiple relationships: drug-drug, target-target, and drug-target. In the feature learning stage, NASNet-DTI adopts a node adaptive learning strategy to dynamically determine the optimal aggregation depth for each node. This ensures that each node can learn the most discriminative features, which effectively alleviates the over-smoothing problem and improves prediction accuracy. Experimental results show that NASNet-DTI significantly outperforms existing methods on multiple datasets, demonstrating its effectiveness and potential as a powerful tool to advance drug discovery and development.
期刊介绍:
Briefings in Bioinformatics is an international journal serving as a platform for researchers and educators in the life sciences. It also appeals to mathematicians, statisticians, and computer scientists applying their expertise to biological challenges. The journal focuses on reviews tailored for users of databases and analytical tools in contemporary genetics, molecular and systems biology. It stands out by offering practical assistance and guidance to non-specialists in computerized methodologies. Covering a wide range from introductory concepts to specific protocols and analyses, the papers address bacterial, plant, fungal, animal, and human data.
The journal's detailed subject areas include genetic studies of phenotypes and genotypes, mapping, DNA sequencing, expression profiling, gene expression studies, microarrays, alignment methods, protein profiles and HMMs, lipids, metabolic and signaling pathways, structure determination and function prediction, phylogenetic studies, and education and training.