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用连续溶剂模型改进基于配体 3D 形状相似性的构象预测。

Improving ligand 3D shape similarity-based pose prediction with a continuum solvent model.

机构信息

Laboratory for Structural Bioinformatics, Center for Biosystems Dynamics Research, RIKEN, 1-7-22 Suehiro, Tsurumi, Yokohama, Kanagawa, 230-0045, Japan.

出版信息

J Comput Aided Mol Des. 2019 Dec;33(12):1045-1055. doi: 10.1007/s10822-019-00220-0. Epub 2019 Aug 28.

Abstract

In order to improve the pose prediction performance of docking methods, we have previously developed the pose prediction using shape similarity (PoPSS) method. It identifies a ligand conformation of the highest shape similarity with target protein crystal ligands. The identified ligand conformation is then placed into the target protein binding pocket and refined using side-chain repacking and Monte Carlo energy minimization. Subsequently, we have reported a modification to PoPSS, named as PoPSS-Lite, using a simple grid-based energy minimization for side-chain repacking and Tversky correlation coefficient as the similarity metric. This modification has improved the pose prediction performance and PoPSS-Lite was one of the top performers in D3R GC3. Here we report a further modification to PoPSS that utilizes a continuum solvent model to account for water mediated protein ligand interactions. In this approach, named as PoPSS-PB, the ligand conformation of the highest shape similarity with crystal ligands is refined along with the target protein binding site by incorporating the Poisson-Boltzmann electrostatics. The performance of PoPSS-PB along with PoPSS and PoPSS-Lite was prospectively evaluated in D3R GC4. PoPSS-PB not only demonstrated excellent performance with mean and median RMSDs of 1.20 and 1.13 Å but also achieved improved performance over PoPSS and PoPSS-Lite. Furthermore, the comparison with other D3R GC4 pose prediction submissions revealed admirable performance. Our results showed that the binding poses of ligands with unknown binding modes can be successfully predicted by utilizing ligand 3D shape similarity with known crystallographic ligands and that taking the solvation into consideration improves pose prediction.

摘要

为了提高对接方法的构象预测性能,我们之前开发了基于形状相似性的构象预测(PoPSS)方法。它识别与靶蛋白晶体配体具有最高形状相似性的配体构象。然后将识别出的配体构象放置到靶蛋白结合口袋中,并通过侧链重新堆积和 Monte Carlo 能量最小化进行精修。随后,我们报告了对 PoPSS 的一种修改,称为 PoPSS-Lite,它使用简单的基于网格的能量最小化进行侧链重新堆积,并使用 Tversky 相关系数作为相似性度量。这种修改提高了构象预测性能,PoPSS-Lite 是 D3R GC3 中的最佳表现者之一。在这里,我们报告了对 PoPSS 的进一步修改,该方法利用连续溶剂模型来考虑水介导的蛋白质配体相互作用。在这种方法中,命名为 PoPSS-PB,与晶体配体具有最高形状相似性的配体构象与靶蛋白结合位点一起通过纳入泊松-玻尔兹曼静电学进行精修。在 D3R GC4 中前瞻性地评估了 PoPSS-PB 与 PoPSS 和 PoPSS-Lite 的性能。PoPSS-PB 不仅表现出出色的性能,平均和中位数 RMSD 分别为 1.20 和 1.13 Å,而且还优于 PoPSS 和 PoPSS-Lite。此外,与其他 D3R GC4 构象预测提交的比较显示出令人钦佩的性能。我们的结果表明,通过利用已知晶体配体的配体 3D 形状相似性,可以成功预测具有未知结合模式的配体的结合构象,并且考虑溶剂化作用可以提高构象预测的准确性。

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