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Theoretical Prediction of the Complex P-Glycoprotein Substrate Efflux Based on the Novel Hierarchical Support Vector Regression Scheme

机译:基于新型分层支持向量回归方案的复杂P-糖蛋白底物外排理论预测

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摘要

P-glycoprotein (P-gp), a membrane-bound transporter, can eliminate xenobiotics by transporting them out of the cells or blood–brain barrier (BBB) at the expense of ATP hydrolysis. Thus, P-gp mediated efflux plays a pivotal role in altering the absorption and disposition of a wide range of substrates. Nevertheless, the mechanism of P-gp substrate efflux is rather complex since it can take place through active transport and passive permeability in addition to multiple P-gp substrate binding sites. A nonlinear quantitative structure–activity relationship (QSAR) model was developed in this study using the novel machine learning-based hierarchical support vector regression (HSVR) scheme to explore the perplexing relationships between descriptors and efflux ratio. The predictions by HSVR were found to be in good agreement with the observed values for the molecules in the training set (n = 50, r2 = 0.96, qCV2 = 0.94, RMSE = 0.10, s = 0.10) and test set (n = 13, q2 = 0.80–0.87, RMSE = 0.21, s = 0.22). When subjected to a variety of statistical validations, the developed HSVR model consistently met the most stringent criteria. A mock test also asserted the predictivity of HSVR. Consequently, this HSVR model can be adopted to facilitate drug discovery and development.
机译:P-糖蛋白(P-gp)是一种与膜结合的转运蛋白,可以通过将异源生物素从细胞或血脑屏障(BBB)中转运出而消除异源生物素,而以ATP水解为代价。因此,P-gp介导的外排在改变各种底物的吸收和沉积方面起着关键作用。然而,P-gp底物外排的机制非常复杂,因为除了多个P-gp底物结合位点外,它还可以通过主动转运和被动渗透发生。在这项研究中,使用新颖的基于机器学习的层次支持向量回归(HSVR)方案开发了非线性定量结构-活动关系(QSAR)模型,以探讨描述子与外排比率之间的困惑关系。发现HSVR的预测与训练集中的分子的观测值非常吻合(n = 50,r 2 = 0.96, q CV 2 = 0.94,RMSE = 0.10,s = 0.10)和测试集(n = 13,q < sup> 2 = 0.80-0.87,RMSE = 0.21,s = 0.22)。经过各种统计验证后,开发的HSVR模型始终符合最严格的标准。一项模拟测试还证实了HSVR的可预测性。因此,可以采用此HSVR模型来促进药物的发现和开发。

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