FSDscore: An Effective Target-focused Scoring Criterion for Virtual Screening.

IF 2.8 4区 医学 Q3 CHEMISTRY, MEDICINAL Molecular Informatics Pub Date : 2023-02-01 DOI:10.1002/minf.202200039
Yi Hua, Dingfang Huang, Li Liang, Xu Qian, Xiaowen Dai, Yuan Xu, Haodi Qiu, Tao Lu, Haichun Liu, Yadong Chen, Yanmin Zhang
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Abstract

Improving screening efficiency is one of the most challenging tasks of virtual screening (VS). In this work, we propose an effective target-focused scoring criterion for VS and apply it to the screening of a specific target scaffold replacement library constructed by enumeration of suitable substitution fragments and R-groups of known ligands. This criterion is based on both ligand- and structure-based scoring methods, which includes feature maps, 3D shape similarity, and the pairwise distance information between proteins and ligands (FSDscore). It is precisely due to the hybrid advantages of ligand- and structure-based approaches that FSDscore performs far better on the validation dataset than other scoring methods. We apply FSDscore to the VS of different kinase targets, MERTK (Mer tyrosine kinase) and ABL1 (tyrosine-protein kinase ABL1) in order to avoid occasionality. Finally, a VS case study shows the potential and effectiveness of our scoring criterion in drug discovery and molecular dynamics simulation further verifies its powerful ability.

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FSDscore:一种有效的以目标为中心的虚拟筛选评分标准。
提高筛选效率是虚拟筛选最具挑战性的任务之一。在这项工作中,我们提出了一个有效的以靶标为中心的VS评分标准,并将其应用于通过枚举合适的取代片段和已知配体的r基构建的特定靶标支架替代库的筛选。该标准基于基于配体和基于结构的评分方法,包括特征图、3D形状相似性和蛋白质与配体之间的成对距离信息(FSDscore)。正是由于基于配体和基于结构的方法的混合优势,FSDscore在验证数据集上的表现远远好于其他评分方法。为了避免偶然性,我们将FSDscore应用于不同激酶靶点MERTK (Mer酪氨酸激酶)和ABL1(酪氨酸蛋白激酶ABL1)的VS。最后,通过VS案例研究表明了我们的评分标准在药物发现和分子动力学模拟中的潜力和有效性,进一步验证了其强大的能力。
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来源期刊
Molecular Informatics
Molecular Informatics CHEMISTRY, MEDICINAL-MATHEMATICAL & COMPUTATIONAL BIOLOGY
CiteScore
7.30
自引率
2.80%
发文量
70
审稿时长
3 months
期刊介绍: Molecular Informatics is a peer-reviewed, international forum for publication of high-quality, interdisciplinary research on all molecular aspects of bio/cheminformatics and computer-assisted molecular design. Molecular Informatics succeeded QSAR & Combinatorial Science in 2010. Molecular Informatics presents methodological innovations that will lead to a deeper understanding of ligand-receptor interactions, macromolecular complexes, molecular networks, design concepts and processes that demonstrate how ideas and design concepts lead to molecules with a desired structure or function, preferably including experimental validation. The journal''s scope includes but is not limited to the fields of drug discovery and chemical biology, protein and nucleic acid engineering and design, the design of nanomolecular structures, strategies for modeling of macromolecular assemblies, molecular networks and systems, pharmaco- and chemogenomics, computer-assisted screening strategies, as well as novel technologies for the de novo design of biologically active molecules. As a unique feature Molecular Informatics publishes so-called "Methods Corner" review-type articles which feature important technological concepts and advances within the scope of the journal.
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