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G4-QuadScreen:一种用于识别针对G-四链体DNA的多靶点导向抗癌先导化合物的计算工具。

G4-QuadScreen: A Computational Tool for Identifying Multi-Target-Directed Anticancer Leads against G-Quadruplex DNA.

作者信息

Bhat-Ambure Jyotsna, Ambure Pravin, Serrano-Candelas Eva, Galiana-Roselló Cristina, Gil-Martínez Ariadna, Guerrero Mario, Martin Margarita, González-García Jorge, García-España Enrique, Gozalbes Rafael

机构信息

MolDrug AI Systems SL, c/Olimpia Arozena Torres, 46018 Valencia, Spain.

ProtoQSAR SL, Centro Europeo de Empresas Innovadoras (CEEI), Parque Tecnológico de Valencia, 46980 Valencia, Spain.

出版信息

Cancers (Basel). 2023 Jul 27;15(15):3817. doi: 10.3390/cancers15153817.

Abstract

The study presents 'G4-QuadScreen', a user-friendly computational tool for identifying MTDLs against G4s. Also, it offers a few hit MTDLs based on in silico and in vitro approaches. Multi-tasking QSAR models were developed using linear discriminant analysis and random forest machine learning techniques for predicting the responses of interest (G4 interaction, G4 stabilization, G4 selectivity, and cytotoxicity) considering the variations in the experimental conditions (e.g., G4 sequences, endpoints, cell lines, buffers, and assays). A virtual screening with G4-QuadScreen and molecular docking using YASARA (AutoDock-Vina) was performed. G4 activities were confirmed via FRET melting, FID, and cell viability assays. Validation metrics demonstrated the high discriminatory power and robustness of the models (the accuracy of all models is ~>90% for the training sets and ~>80% for the external sets). The experimental evaluations showed that ten screened MTDLs have the capacity to selectively stabilize multiple G4s. Three screened MTDLs induced a strong inhibitory effect on various human cancer cell lines. This pioneering computational study serves a tool to accelerate the search for new leads against G4s, reducing false positive outcomes in the early stages of drug discovery. The G4-QuadScreen tool is accessible on the ChemoPredictionSuite website.

摘要

该研究展示了“G4-QuadScreen”,这是一种用于识别针对G4的多靶点药物配体的用户友好型计算工具。此外,它还基于计算机模拟和体外方法提供了一些命中的多靶点药物配体。使用线性判别分析和随机森林机器学习技术开发了多任务定量构效关系模型,以预测感兴趣的反应(G4相互作用、G4稳定化、G4选择性和细胞毒性),同时考虑实验条件的变化(例如,G4序列、终点、细胞系、缓冲液和检测方法)。使用G4-QuadScreen进行了虚拟筛选,并使用YASARA(AutoDock-Vina)进行了分子对接。通过荧光共振能量转移熔解、荧光检测和细胞活力检测确认了G4活性。验证指标证明了模型具有高辨别力和稳健性(所有模型对训练集的准确率约>90%,对外部集的准确率约>80%)。实验评估表明,筛选出的10种多靶点药物配体有能力选择性地稳定多种G4。筛选出的3种多靶点药物配体对多种人类癌细胞系产生了强烈的抑制作用。这项开创性的计算研究为加速寻找针对G4的新先导化合物提供了一种工具,减少了药物发现早期阶段的假阳性结果。G4-QuadScreen工具可在ChemoPredictionSuite网站上获取。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1186/10416877/fe1e339f4d31/cancers-15-03817-g001.jpg

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