通过双药视觉表征预测药物-药物相互作用。

IF 5.3 2区 化学 Q1 CHEMISTRY, MEDICINAL
Lingxuan Xie,Tengfei Ma,Yuqin He,Yiping Liu,Xiangxiang Zeng
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引用次数: 0

摘要

药物相互作用预测是保证用药安全和治疗效果的重要手段。虽然现有的模型通常依赖于化学描述符或分子图,但它们往往忽略了嵌入在视觉分子中的丰富的空间和结构线索。为了解决这个问题,我们提出了一种新的基于视觉的框架DDVR-DDI,它通过将药物对编码为单个融合的分子图像来预测ddi,从而可以直接建模它们潜在的相互作用界面。为了增强视觉药物对的表征学习,我们引入了一种两阶段的自监督预训练策略:位置不变的对比任务提高了对不同空间变化下某些药物对的理解,而拼图任务则促进了对细粒度结构的理解。此外,我们开发了一个多专家投票机制,其中多个模型分析每个药物对的不同增强视图,以通过集成推理提高预测的准确性和稳定性。在基准DDI数据集上进行的大量实验表明,我们的模型达到了最先进的性能。为了进一步解释其预测,我们采用了Grad-CAM可视化,并进行了多次实验来验证模型的稳定性和可解释性;此外,我们对利托那韦对CYP3A的抑制进行了案例研究,发现我们的模型始终突出化学上重要的亚结构。这些发现强调了基于图像的建模在药物相互作用研究中的准确预测和机制洞察的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Predicting Drug-Drug Interaction via Dual-Drug Visual Representation.
Drug-drug interaction (DDI) prediction is essential for ensuring medication safety and therapeutic efficacy. While existing models often rely on chemical descriptors or molecular graphs, they tend to overlook the rich spatial and structural cues embedded in visual molecules. To address this issue, we propose DDVR-DDI, a novel vision-based framework that predicts DDIs by encoding drug pairs as a single fused molecular image, enabling direct modeling of their potential interaction interface. To enhance representation learning of visual drug pairs, we introduce a two-stage self-supervised pretraining strategy: a position-invariant contrastive task improves understanding of certain drug pairs in different spatial variations, while a jigsaw puzzle task encourages fine-grained structural understanding. Additionally, we develop a multiexpert voting mechanism, where multiple models analyze distinct augmented views of each drug pair to boost prediction accuracy and stability through ensemble inference. Extensive experiments on benchmark DDI data sets show that our model achieves state-of-the-art performance. To further interpret its predictions, we employ Grad-CAM visualizations and conduct multiple experiments to validate the stability and interpretability of the model; furthermore, we conduct a case study on Ritonavir inhibition of CYP3A, revealing that our model consistently highlights chemically significant substructures. These findings underscore the potential of image-based modeling for both accurate prediction and mechanistic insight in drug interaction research.
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来源期刊
CiteScore
9.80
自引率
10.70%
发文量
529
审稿时长
1.4 months
期刊介绍: The Journal of Chemical Information and Modeling publishes papers reporting new methodology and/or important applications in the fields of chemical informatics and molecular modeling. Specific topics include the representation and computer-based searching of chemical databases, molecular modeling, computer-aided molecular design of new materials, catalysts, or ligands, development of new computational methods or efficient algorithms for chemical software, and biopharmaceutical chemistry including analyses of biological activity and other issues related to drug discovery. Astute chemists, computer scientists, and information specialists look to this monthly’s insightful research studies, programming innovations, and software reviews to keep current with advances in this integral, multidisciplinary field. As a subscriber you’ll stay abreast of database search systems, use of graph theory in chemical problems, substructure search systems, pattern recognition and clustering, analysis of chemical and physical data, molecular modeling, graphics and natural language interfaces, bibliometric and citation analysis, and synthesis design and reactions databases.
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