MFE-DDI:药物-药物相互作用预测的多视图特征编码框架。

IF 4.4 2区 生物学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY
Computational and structural biotechnology journal Pub Date : 2025-05-26 eCollection Date: 2025-01-01 DOI:10.1016/j.csbj.2025.05.029
Lingfeng Wang, Yinghong Li, Yaozheng Zhou, Liping Guo, Congzhou Chen
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引用次数: 0

摘要

长期以来,多药联合治疗一直是利用药物之间的协同作用治疗复杂疾病的重要方法。然而,药物-药物相互作用(ddi)并不总是有益的。准确和快速识别ddi对于减轻药物相关副作用至关重要。目前,许多基于计算的方法已被用于加速ddi的预测。然而,这些方法大多采用单一视角获取药物特征,表达能力有限,不能完全代表药物的本质属性。在本研究中,我们提出了基于多视图特征嵌入的药物-药物相互作用预测(MFE-DDI)方法,该方法将smile信息、分子图数据和原子空间语义信息整合在一起,从多个角度对药物进行建模,并封装对药物相互作用预测至关重要的复杂药物信息。同时,将不同特征编码通道提取的特征信息融合到基于注意力的融合模块中,充分传达药物的本质。因此,该方法提高了DDI预测任务的有效性。实验结果表明,MFE-DDI方法在三个数据集上优于其他基线方法。分析实验证明了模型的鲁棒性和模型各组成部分的必要性。对新批准药物的案例研究证明了我们的方法在实际情况下的有效性。在MFE-DDI中使用的代码和数据可以在https://github.com/2019040445/MFE_DDI上找到。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MFE-DDI: A multi-view feature encoding framework for drug-drug interaction prediction.

Multidrug combination therapy has long been a vital approach for treating complex diseases by leveraging synergistic effects between drugs. However, drug-drug interactions (DDIs) are not uniformly beneficial. Accurate and rapid identification of DDIs is critical to mitigate drug-related side effects. Currently, many computational-based methods have been used to expedite the prediction of DDIs. However, most of these methods use a single perspective to obtain drug features, which have limited expressive capabilities and cannot fully represent the essential attributes of drugs. In this study, we propose the Multi-view Feature Embedding for drug-drug interaction prediction (MFE-DDI), which integrates SMILES information, molecular graph data and atom spatial semantic information to model drugs from multiple perspectives and encapsulate the intricate drug information crucial for predicting DDIs. Concurrently, the feature information extracted from different feature encoding channels is fused in the attention-based fusion module to fully convey the essence of drugs. Consequently, this approach enhances the efficacy of the DDI prediction task. Experimental results indicate that MFE-DDI surpasses other baseline methods on three datasets. Moreover, analysis experiments demonstrate the robustness of the model and the necessity of each component of the model. Case studies on newly approved drugs demonstrate the effectiveness of our method in real scenarios. The code and data used in MFE-DDI can be found at https://github.com/2019040445/MFE_DDI.

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来源期刊
Computational and structural biotechnology journal
Computational and structural biotechnology journal Biochemistry, Genetics and Molecular Biology-Biophysics
CiteScore
9.30
自引率
3.30%
发文量
540
审稿时长
6 weeks
期刊介绍: Computational and Structural Biotechnology Journal (CSBJ) is an online gold open access journal publishing research articles and reviews after full peer review. All articles are published, without barriers to access, immediately upon acceptance. The journal places a strong emphasis on functional and mechanistic understanding of how molecular components in a biological process work together through the application of computational methods. Structural data may provide such insights, but they are not a pre-requisite for publication in the journal. Specific areas of interest include, but are not limited to: Structure and function of proteins, nucleic acids and other macromolecules Structure and function of multi-component complexes Protein folding, processing and degradation Enzymology Computational and structural studies of plant systems Microbial Informatics Genomics Proteomics Metabolomics Algorithms and Hypothesis in Bioinformatics Mathematical and Theoretical Biology Computational Chemistry and Drug Discovery Microscopy and Molecular Imaging Nanotechnology Systems and Synthetic Biology
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