• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

用于药物-靶点相互作用预测的邻域正则化逻辑矩阵分解

Neighborhood Regularized Logistic Matrix Factorization for Drug-Target Interaction Prediction.

作者信息

Liu Yong, Wu Min, Miao Chunyan, Zhao Peilin, Li Xiao-Li

机构信息

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.

出版信息

PLoS Comput Biol. 2016 Feb 12;12(2):e1004760. doi: 10.1371/journal.pcbi.1004760. eCollection 2016 Feb.

DOI:10.1371/journal.pcbi.1004760
PMID:26872142
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4752318/
Abstract

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.

摘要

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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/dea4312d8d16/pcbi.1004760.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/1849a44b9338/pcbi.1004760.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/644030017fb9/pcbi.1004760.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/58d41d701ae4/pcbi.1004760.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/e3a921205b92/pcbi.1004760.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/c71f054e6415/pcbi.1004760.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/86c9ee128f41/pcbi.1004760.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/71f44fc4d3a1/pcbi.1004760.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/dea4312d8d16/pcbi.1004760.g008.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/1849a44b9338/pcbi.1004760.g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/644030017fb9/pcbi.1004760.g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/58d41d701ae4/pcbi.1004760.g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/e3a921205b92/pcbi.1004760.g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/c71f054e6415/pcbi.1004760.g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/86c9ee128f41/pcbi.1004760.g006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/71f44fc4d3a1/pcbi.1004760.g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/cef4/4752318/dea4312d8d16/pcbi.1004760.g008.jpg

相似文献

1
Neighborhood Regularized Logistic Matrix Factorization for Drug-Target Interaction Prediction.用于药物-靶点相互作用预测的邻域正则化逻辑矩阵分解
PLoS Comput Biol. 2016 Feb 12;12(2):e1004760. doi: 10.1371/journal.pcbi.1004760. eCollection 2016 Feb.
2
Drug-Target Interaction Prediction with Graph Regularized Matrix Factorization.基于图正则化矩阵分解的药物-靶点相互作用预测
IEEE/ACM Trans Comput Biol Bioinform. 2017 May-Jun;14(3):646-656. doi: 10.1109/TCBB.2016.2530062. Epub 2016 Feb 15.
3
Drug-target interaction prediction using Multi Graph Regularized Nuclear Norm Minimization.基于多图正则化核范数最小化的药物-靶点相互作用预测。
PLoS One. 2020 Jan 16;15(1):e0226484. doi: 10.1371/journal.pone.0226484. eCollection 2020.
4
Drug-target interaction prediction via class imbalance-aware ensemble learning.通过类不平衡感知集成学习进行药物-靶点相互作用预测。
BMC Bioinformatics. 2016 Dec 22;17(Suppl 19):509. doi: 10.1186/s12859-016-1377-y.
5
NRLMF: Beta-distribution-rescored neighborhood regularized logistic matrix factorization for improving the performance of drug-target interaction prediction.NRLMF:用于改进药物-靶点相互作用预测性能的β分布重新评分邻域正则化逻辑矩阵分解
Biochem Biophys Rep. 2019 Feb 7;18:100615. doi: 10.1016/j.bbrep.2019.01.008. eCollection 2019 Jul.
6
LPI-NRLMF: lncRNA-protein interaction prediction by neighborhood regularized logistic matrix factorization.LPI-NRLMF:基于邻域正则化逻辑矩阵分解的长链非编码RNA-蛋白质相互作用预测
Oncotarget. 2017 Oct 19;8(61):103975-103984. doi: 10.18632/oncotarget.21934. eCollection 2017 Nov 28.
7
De Novo Prediction of Drug-Target Interactions Using Laplacian Regularized Schatten -Norm Minimization.
J Comput Biol. 2021 Jul;28(7):660-673. doi: 10.1089/cmb.2020.0538. Epub 2021 Jan 21.
8
Graph regularized non-negative matrix factorization with prior knowledge consistency constraint for drug-target interactions prediction.基于先验知识一致性约束的图正则化非负矩阵分解在药物-靶标相互作用预测中的应用。
BMC Bioinformatics. 2022 Dec 29;23(1):564. doi: 10.1186/s12859-022-05119-6.
9
Drug-Target Interaction Prediction via Dual Laplacian Graph Regularized Logistic Matrix Factorization.通过双拉普拉斯图正则化逻辑矩阵分解进行药物-靶点相互作用预测
Biomed Res Int. 2021 Mar 26;2021:5599263. doi: 10.1155/2021/5599263. eCollection 2021.
10
Inferring Interactions between Novel Drugs and Novel Targets via Instance-Neighborhood-Based Models.通过基于实例邻域的模型推断新型药物与新型靶点之间的相互作用。
Curr Protein Pept Sci. 2018;19(5):488-497. doi: 10.2174/1389203718666161108093907.

引用本文的文献

1
Accurate prediction of drug-protein interactions by maintaining the original topological relationships among embeddings.通过保持嵌入之间的原始拓扑关系来准确预测药物-蛋白质相互作用。
BMC Biol. 2025 Aug 5;23(1):243. doi: 10.1186/s12915-025-02338-0.
2
Drug-target interaction prediction based on graph convolutional autoencoder with dynamic weighting residual GCN.基于具有动态加权残差图卷积网络的图卷积自动编码器的药物-靶点相互作用预测
BMC Bioinformatics. 2025 Jul 29;26(1):200. doi: 10.1186/s12859-025-06198-x.
3
CPI-MIF: Compound-Protein Interaction Prediction with Multiview Information Fusion.

本文引用的文献

1
Kernelized Bayesian Matrix Factorization.核化贝叶斯矩阵分解。
IEEE Trans Pattern Anal Mach Intell. 2014 Oct;36(10):2047-60. doi: 10.1109/TPAMI.2014.2313125.
2
A survey on the computational approaches to identify drug targets in the postgenomic era.后基因组时代用于识别药物靶点的计算方法综述。
Biomed Res Int. 2015;2015:239654. doi: 10.1155/2015/239654. Epub 2015 Apr 28.
3
Integration of molecular network data reconstructs Gene Ontology.分子网络数据的整合重建了基因本体论。
CPI-MIF:基于多视图信息融合的复合蛋白相互作用预测
ACS Omega. 2025 Jul 13;10(28):30155-30166. doi: 10.1021/acsomega.5c00113. eCollection 2025 Jul 22.
4
DTI-RME: a robust and multi-kernel ensemble approach for drug-target interaction prediction.DTI-RME:一种用于药物-靶点相互作用预测的稳健多内核集成方法。
BMC Biol. 2025 Jul 28;23(1):225. doi: 10.1186/s12915-025-02340-6.
5
DTGHAT: multi-molecule heterogeneous graph transformer based on multi-molecule graph for drug-target identification.DTGHAT:基于多分子图的用于药物靶点识别的多分子异构图变换器
Front Pharmacol. 2025 Apr 28;16:1596216. doi: 10.3389/fphar.2025.1596216. eCollection 2025.
6
DMGAT: predicting ncRNA-drug resistance associations based on diffusion map and heterogeneous graph attention network.DMGAT:基于扩散映射和异构图注意力网络预测非编码RNA与耐药性的关联
Brief Bioinform. 2025 Mar 4;26(2). doi: 10.1093/bib/bbaf179.
7
A novel approach for target deconvolution from phenotype-based screening using knowledge graph.一种使用知识图谱从基于表型的筛选中进行靶点反卷积的新方法。
Sci Rep. 2025 Jan 18;15(1):2414. doi: 10.1038/s41598-025-86166-w.
8
Enhancing drug-target interaction predictions in context of neurodegenerative diseases using bidirectional long short-term memory in male Swiss albino mice pharmaco-EEG analysis.在雄性瑞士白化小鼠药物脑电图分析中使用双向长短期记忆增强神经退行性疾病背景下的药物-靶点相互作用预测
Heliyon. 2024 Oct 28;10(21):e39279. doi: 10.1016/j.heliyon.2024.e39279. eCollection 2024 Nov 15.
9
Drug-target interaction prediction through fine-grained selection and bidirectional random walk methodology.通过细粒度选择和双向随机游走方法进行药物-靶标相互作用预测。
Sci Rep. 2024 Aug 5;14(1):18104. doi: 10.1038/s41598-024-69186-w.
10
GSRF-DTI: a framework for drug-target interaction prediction based on a drug-target pair network and representation learning on a large graph.GSRF-DTI:一种基于药物-靶点对网络和大图表示学习的药物-靶点相互作用预测框架。
BMC Biol. 2024 Jul 18;22(1):156. doi: 10.1186/s12915-024-01949-3.
Bioinformatics. 2014 Sep 1;30(17):i594-600. doi: 10.1093/bioinformatics/btu470.
4
DINIES: drug-target interaction network inference engine based on supervised analysis.基于监督分析的药物-靶标相互作用网络推理引擎。
Nucleic Acids Res. 2014 Jul;42(Web Server issue):W39-45. doi: 10.1093/nar/gku337. Epub 2014 May 16.
5
Toward more realistic drug-target interaction predictions.迈向更现实的药物-靶点相互作用预测。
Brief Bioinform. 2015 Mar;16(2):325-37. doi: 10.1093/bib/bbu010. Epub 2014 Apr 9.
6
Predicting drug-target interactions using probabilistic matrix factorization.使用概率矩阵分解预测药物-靶点相互作用。
J Chem Inf Model. 2013 Dec 23;53(12):3399-409. doi: 10.1021/ci400219z. Epub 2013 Dec 10.
7
Prediction of drug-target interactions for drug repositioning only based on genomic expression similarity.仅基于基因组表达相似性预测药物重定位的药物-靶标相互作用。
PLoS Comput Biol. 2013;9(11):e1003315. doi: 10.1371/journal.pcbi.1003315. Epub 2013 Nov 7.
8
Similarity-based machine learning methods for predicting drug-target interactions: a brief review.基于相似度的机器学习方法在药物-靶标相互作用预测中的研究进展。
Brief Bioinform. 2014 Sep;15(5):734-47. doi: 10.1093/bib/bbt056. Epub 2013 Aug 11.
9
Predicting Drug-Target Interactions for New Drug Compounds Using a Weighted Nearest Neighbor Profile.使用加权最近邻轮廓预测新药物化合物的药物-靶点相互作用
PLoS One. 2013 Jun 26;8(6):e66952. doi: 10.1371/journal.pone.0066952. Print 2013.
10
Drug-target interaction prediction by learning from local information and neighbors.基于局部信息和邻居学习的药物-靶标相互作用预测。
Bioinformatics. 2013 Jan 15;29(2):238-45. doi: 10.1093/bioinformatics/bts670. Epub 2012 Nov 17.