Combining pharmacophore models derived from DNA-encoded chemical libraries with structure-based exploration to predict Tankyrase 1 inhibitors

药效团 化学 化学空间 药物发现 配体效率 计算生物学 化学图书馆 配体(生物化学) 连接器 组合化学 小分子 DNA 虚拟筛选 靶蛋白 立体化学 生物化学 计算机科学 生物 受体 操作系统 基因
作者
Alba L. Montoya,Marta Glavatskikh,Brayden J. Halverson,Lik Hang Yuen,H. Schüler,Dmitri Kireev,Raphael M. Franzini
出处
期刊:European journal of medicinal chemistry [Elsevier BV]
卷期号:246: 114980-114980 被引量:13
标识
DOI:10.1016/j.ejmech.2022.114980
摘要

DNA-encoded chemical libraries (DECLs) interrogate the interactions of a target of interest with vast numbers of molecules. DECLs hence provide abundant information about the chemical ligand space for therapeutic targets, and there is considerable interest in methods for exploiting DECL screening data to predict novel ligands. Here we introduce one such approach and demonstrate its feasibility using the cancer-related poly-(ADP-ribose)transferase tankyrase 1 (TNKS1) as a model target. First, DECL affinity selections resulted in structurally diverse TNKS1 inhibitors with high potency including compound 2 with an IC50 value of 0.8 nM. Additionally, TNKS1 hits from four DECLs were translated into pharmacophore models, which were exploited in combination with docking-based screening to identify TNKS1 ligand candidates in databases of commercially available compounds. This computational strategy afforded TNKS1 inhibitors that are outside the chemical space covered by the DECLs and yielded the drug-like lead compound 12 with an IC50 value of 22 nM. The study further provided insights in the reliability of screening data and the effect of library design on hit compounds. In particular, the study revealed that while in general DECL screening data are in good agreement with off-DNA ligand binding, unpredictable interactions of the DNA-attachment linker with the target protein contribute to the noise in the affinity selection data.
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