A new redundant variable pruning approach—minor latent variable perturbation–PLS used for QSAR studies on anti-HIV drugs

Hong-Ping Xie , Jian-Hui Jiang , Hui Cui , Guo-Li Shen , Ru-Qin Yu
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引用次数: 12

Abstract

A new approach for eliminating the redundant variables in the multivariable data matrix encountered in QSAR studies, minor latent variable perturbation (MLVP)-PLS method has been proposed. In the latent variable (LV) space, the minor latent variables (LVs) with small covariances are mainly formulated by linear combinations of the redundant variables including information-deficient and highly correlative ones, while the major LVs with large covariances are mainly contributed by the informative variables. Deleting a minor LV, which is equivalent to a perturbation for LV space, could make the redundant variables not well be represented in LV subspace, leading to strong variation of their PLS regression coefficients. The informative variables could still be normally represented in LV subspace with the PLS regression coefficients remaining relatively stable. MLVP-PLS utilizes this fact to discriminate the informative and redundant variables. It gradually identifies and eliminates the redundant variables according to the relative variation of PLS regression coefficients after perturbations are given. The elimination process is terminated according to some proposed criteria. Applying the method to the quantitative structure–activity relationship (QSAR) studies on TIBO derivatives as potential anti-HIV drugs has demonstrated the feasibility and robustness of the proposed approach. A deeper insight into the effect of different structural parameters on the bio-activity of TIBO derivatives has been reached.

一种新的冗余变量修剪方法-微小潜在变量扰动- pls用于抗hiv药物的QSAR研究
提出了一种消除QSAR研究中所遇到的多变量数据矩阵中冗余变量的新方法——小潜变量摄动(MLVP)-PLS方法。在潜变量空间中,协方差较小的次要潜变量主要由信息缺失和高度相关等冗余变量的线性组合构成,协方差较大的主要潜变量主要由信息丰富的变量构成。删除一个较小的LV相当于对LV空间的扰动,会使冗余变量在LV子空间中不能很好地表示,从而导致其PLS回归系数的强烈变化。信息变量仍然可以在LV子空间中正常表示,PLS回归系数保持相对稳定。MLVP-PLS利用这一事实来区分信息和冗余变量。在给定扰动后,根据PLS回归系数的相对变化,逐步识别和消除冗余变量。根据一些建议的标准终止淘汰过程。将该方法应用于TIBO衍生物作为潜在抗hiv药物的定量构效关系(QSAR)研究,证明了该方法的可行性和鲁棒性。对不同结构参数对TIBO衍生物生物活性的影响有了更深入的了解。
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