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吲哚啉的氨磺酰苯基衍生物对CDK-2和GSK-3β的抑制机制——一项分子动力学研究

Inhibition mechanism of CDK-2 and GSK-3β by a sulfamoylphenyl derivative of indoline-a molecular dynamics study.

作者信息

Czeleń Przemysław

机构信息

Department of Physical Chemistry, Faculty of Pharmacy, Collegium Medicum, Nicolaus Copernicus University, Kurpinskiego 5, 85-096, Bydgoszcz, Poland.

出版信息

J Mol Model. 2017 Aug;23(8):230. doi: 10.1007/s00894-017-3395-8. Epub 2017 Jul 19.

Abstract

A good understanding of the inhibition mechanism of enzymes exhibiting high levels of similarity is the first step to the discovery of new drugs with selective potential. Examples of such proteins include glycogen synthase kinase-3 (GSK-3β) and cyclin-dependent kinase 2 (CDK-2). This article reports the mechanism of such enzyme inhibition as analyzed by an indoline sulfamylophenyl derivative (CHEMBL410072). Previous work has shown that such compounds exhibit selective properties towards their biological targets. This study used a combined procedure involving docking and molecular dynamics simulations, which allowed identification of interactions responsible for stabilization of complexes, and analysis of the dynamic stability of the systems obtained. The initial data obtained during the molecular docking stage show that the ligand molecule exhibits a similar affinity towards both active sites, which was confirmed by quantification of identified interactions and energy values. However, the data do not cover dynamic aspects of the considered systems. Molecular dynamics simulations realized for both complexes indicate significant dissimilarities in dynamics properties of both side chains of the considered ligands, especially in the case of the part containing the sulfamide group. Such increased mobility of the analyzed systems disrupts the stability of binding in the stabilized complex with GSK-3β protein, which finally affects also the binding affinity of the ligand molecule towards this enzyme.

摘要

深入了解具有高度相似性的酶的抑制机制是发现具有选择性潜力的新药的第一步。这类蛋白质的例子包括糖原合酶激酶-3(GSK-3β)和细胞周期蛋白依赖性激酶2(CDK-2)。本文报道了一种吲哚啉磺酰基苯基衍生物(CHEMBL410072)对这类酶抑制作用的机制。先前的研究表明,这类化合物对其生物靶点具有选择性。本研究采用了对接和分子动力学模拟相结合的方法,该方法能够识别负责复合物稳定的相互作用,并分析所得系统的动态稳定性。在分子对接阶段获得的初始数据表明,配体分子对两个活性位点表现出相似的亲和力,这一点通过对已识别的相互作用和能量值进行量化得到了证实。然而,这些数据并未涵盖所考虑系统的动态方面。对两种复合物进行的分子动力学模拟表明,所考虑配体的两条侧链在动力学性质上存在显著差异,特别是在含有磺酰胺基团的部分。所分析系统的这种增加的流动性破坏了与GSK-3β蛋白形成的稳定复合物中结合的稳定性,最终也影响了配体分子对该酶的结合亲和力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/db80/5517586/2ae4636fc933/894_2017_3395_Fig1_HTML.jpg

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