Liu Yong, Wu Min, Miao Chunyan, Zhao Peilin, Li Xiao-Li
Joint NTU-UBC Research Centre of Excellence in Active Living for the Elderly (LILY), and School of Computer Engineering, Nanyang Technological University, Singapore.
Institute for Infocomm Research (I2R), Agency for Science, Technology and Research (A*STAR), Singapore.
PLoS Comput Biol. 2016 Feb 12;12(2):e1004760. doi: 10.1371/journal.pcbi.1004760. eCollection 2016 Feb.
In pharmaceutical sciences, a crucial step of the drug discovery process is the identification of drug-target interactions. However, only a small portion of the drug-target interactions have been experimentally validated, as the experimental validation is laborious and costly. To improve the drug discovery efficiency, there is a great need for the development of accurate computational approaches that can predict potential drug-target interactions to direct the experimental verification. In this paper, we propose a novel drug-target interaction prediction algorithm, namely neighborhood regularized logistic matrix factorization (NRLMF). Specifically, the proposed NRLMF method focuses on modeling the probability that a drug would interact with a target by logistic matrix factorization, where the properties of drugs and targets are represented by drug-specific and target-specific latent vectors, respectively. Moreover, NRLMF assigns higher importance levels to positive observations (i.e., the observed interacting drug-target pairs) than negative observations (i.e., the unknown pairs). Because the positive observations are already experimentally verified, they are usually more trustworthy. Furthermore, the local structure of the drug-target interaction data has also been exploited via neighborhood regularization to achieve better prediction accuracy. We conducted extensive experiments over four benchmark datasets, and NRLMF demonstrated its effectiveness compared with five state-of-the-art approaches.
在药物科学领域,药物发现过程中的一个关键步骤是识别药物与靶点的相互作用。然而,只有一小部分药物与靶点的相互作用得到了实验验证,因为实验验证既费力又昂贵。为了提高药物发现的效率,迫切需要开发精确的计算方法,能够预测潜在的药物与靶点的相互作用,以指导实验验证。在本文中,我们提出了一种新颖的药物与靶点相互作用预测算法,即邻域正则化逻辑矩阵分解(NRLMF)。具体而言,所提出的NRLMF方法专注于通过逻辑矩阵分解对药物与靶点相互作用的概率进行建模,其中药物和靶点的属性分别由药物特异性和靶点特异性潜在向量表示。此外,NRLMF对正观测值(即观测到的相互作用的药物与靶点对)赋予比对负观测值(即未知对)更高的重要性水平。由于正观测值已经经过实验验证,它们通常更值得信赖。此外,还通过邻域正则化利用了药物与靶点相互作用数据的局部结构,以实现更好的预测准确性。我们在四个基准数据集上进行了广泛的实验,与五种最先进的方法相比,NRLMF证明了其有效性。