计算机科学
人工智能
机器学习
图形
深度学习
卷积神经网络
源代码
一般化
水准点(测量)
药物发现
软件可移植性
模式
编码(集合论)
交互网络
过程(计算)
序列(生物学)
循环神经网络
特征学习
人工神经网络
药物靶点
注意力网络
训练集
作者
Qiufen Chen,Guanyan Nie,Xiaoli Li,Ying Xu,Chris Soon Heng Tan
标识
DOI:10.1021/acs.jcim.5c02283
摘要
Accurate prediction of drug-target interactions (DTIs) is essential for drug discovery and repurposing. Despite recent advances, deep learning models often exhibit limited generalization under realistic cold-start scenarios and suffer from poor interpretability. To address these challenges, we present BioFusionDTI, a multimodal deep learning framework that integrates graph-based and sequence-based representations of drugs and proteins. BioFusionDTI employs graph convolutional networks (GCNs) to extract structural features from molecular and protein graphs, and convolutional neural networks (CNNs) to process sequence embeddings derived from pretrained biomolecular language models. A bilinear attention network (BAN) is further introduced to capture fine-grained cross-modal interactions, thereby enhancing predictive accuracy and interpretability. Extensive experiments on three benchmark data sets (SNAP, DRH, and Kinase) under warm, cold-drug, and cold-protein settings demonstrate that BioFusionDTI consistently outperforms state-of-the-art baselines. Ablation studies highlight the effectiveness of the fusion strategy, with the BAN module making a substantial contribution to performance gains. Moreover, attention visualizations reveal biologically plausible interaction sites, in agreement with molecular docking results. The present study suggests that BioFusionDTI is a robust and interpretable tool for drug discovery and repositioning. The source code is available at https://github.com/QiufenChen/BioFusionDTI.
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