MFCADTI:通过交叉注意机制整合多种特征,提高药物-靶标相互作用预测。

IF 2.9 3区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Na Quan, Shicheng Ma, Kai Zhao, Xuehua Bi, Linlin Zhang
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引用次数: 0

摘要

准确识别潜在的药物-靶标相互作用(DTIs)是药物发现的关键步骤。多种异质生物数据为DTI预测提供了丰富的特征。基于这些数据提出了许多计算方法。然而,这些方法大多是从序列或网络中提取特征,只利用药物和靶点特征的一个方面,而忽略了这两种特征之间的互补信息。事实上,整合不同类型的特征将为DTI预测提供更有价值的信息。在本文中,我们提出了一种新的方法,即MFCADTI,通过交叉注意机制集成多源特征来提高dti的预测能力。该方法从异构网络中提取网络拓扑特征,从药物和靶点序列中提取属性特征。考虑到网络和属性特征之间的互补性和异质性,交叉注意机制将药物和靶点的网络和属性特征整合起来。为了捕捉药物和靶标之间的相关性,交叉注意被用来学习每个药物-靶标对的相互作用特征。我们在两个数据集上对MFCADTI进行了评估,实验结果表明,与最先进的方法相比,MFCADTI的性能有了显着提高。最后,案例研究表明,MFCADTI是一种有效的DTI预测方法,可为药物开发提供有价值的指导。本研究使用的数据和源代码可在https://github.com/Dejavun/MFCADTI上获得。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
MFCADTI: improving drug-target interaction prediction by integrating multiple feature through cross attention mechanism.

Accurately identifying potential drug-target interactions (DTIs) is a critical step in drug discovery. Multiple heterogeneous biological data provide abundant features for DTI prediction. Many computational methods have been proposed based on these data. However, most of these methods either extract features from sequences or from networks, utilizing only one aspect of the characteristics of drugs and targets, neglecting the complementary information between these two types of features. In fact, integrating different types of features will provide more valuable information for DTI prediction. In this article, we propose a novel method to improve the predictive capability for DTIs, named MFCADTI, by integrating multi-source feature through cross-attention mechanisms. The method extracts network topological features from the heterogeneous network and attribute features from sequences of drugs and targets. Considering the complementarity and heterogeneity between network and attribute features, cross-attention mechanisms are used to integrate the network and attribute features of drugs and targets. To capture the correlations between drugs and targets, cross-attention is used to learn the interaction features of each drug-target pair. We evaluate MFCADTI on two datasets and experimental results demonstrate a significant improvement in the performance of MFCADTI compared to state-of-the-art methods. Finally, case studies illustrate that MFCADTI is an effective DTI prediction way that provides valuable guidance for drug development. The data and source code used in this study are available at: https://github.com/Dejavun/MFCADTI .

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来源期刊
BMC Bioinformatics
BMC Bioinformatics 生物-生化研究方法
CiteScore
5.70
自引率
3.30%
发文量
506
审稿时长
4.3 months
期刊介绍: BMC Bioinformatics is an open access, peer-reviewed journal that considers articles on all aspects of the development, testing and novel application of computational and statistical methods for the modeling and analysis of all kinds of biological data, as well as other areas of computational biology. BMC Bioinformatics is part of the BMC series which publishes subject-specific journals focused on the needs of individual research communities across all areas of biology and medicine. We offer an efficient, fair and friendly peer review service, and are committed to publishing all sound science, provided that there is some advance in knowledge presented by the work.
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