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以天然药物靶向AMPK信号通路用于动脉粥样硬化治疗:计算机模拟筛选与体外试验的整合

Targeting AMPK signalling pathway with natural medicines for atherosclerosis therapy: an integration of in silico screening and in vitro assay.

作者信息

Ou Tiantong, Hou Xumin, Guan Shaofeng, Dai Jinjie, Han Wenzheng, Li Ruogu, Wang Wenxia, Qu Xinkai, Zhang Min

机构信息

a Cardiology Department of Shanghai Chest Hospital , Shanghai Jiaotong University , 241 West Huaihai Road, Shanghai 200030 , P.R. China.

出版信息

Nat Prod Res. 2016 Jun;30(11):1240-7. doi: 10.1080/14786419.2015.1050672. Epub 2015 Jul 13.

Abstract

An integration of virtual screening and kinase assay was reported to identify AMPK kinase inhibitors from various natural medicines.The activation of AMP-activated protein kinase (AMPK) signalling pathway plays a central role in the pathologic progression of atherosclerosis (AS). Targeting the AMPK is thus considered as a potential therapeutics to attenuate AS. Here, we report the establishment of a synthetic pipeline that integrates in silico virtual screening and in vitro kinase assay to discover new lead compounds of AMPK inhibitors. The screening is performed against a large-size pool of structurally diverse natural products, from which a number of compounds are inferred as promising candidates, and few of them are further tested in vitro by using a standard kinase assay protocol to determine their inhibitory potency against AMPK. With this scheme we successfully identify five potent AMPK inhibitors with IC50 values at micromolar level. We also examine the structural basis and molecular mechanism of nonbonded interaction network across the modelled complex interface of AMPK kinase domain with a newly identified natural medicine.

摘要

据报道,虚拟筛选和激酶测定相结合可从各种天然药物中鉴定出AMPK激酶抑制剂。AMP激活的蛋白激酶(AMPK)信号通路的激活在动脉粥样硬化(AS)的病理进展中起核心作用。因此,靶向AMPK被认为是减轻AS的一种潜在治疗方法。在此,我们报告了一种合成流程的建立,该流程整合了计算机虚拟筛选和体外激酶测定,以发现AMPK抑制剂的新先导化合物。针对大量结构多样的天然产物进行筛选,从中推断出许多化合物为有前景的候选物,并使用标准激酶测定方案在体外对其中少数化合物进行进一步测试,以确定它们对AMPK的抑制效力。通过该方案,我们成功鉴定出五种IC50值处于微摩尔水平的强效AMPK抑制剂。我们还研究了AMPK激酶结构域与一种新鉴定的天然药物的模拟复合物界面上非键相互作用网络的结构基础和分子机制。

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