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探索地灭蝇胺在昆虫 GABA 受体中的相互作用机制及通过模拟筛选潜在的拮抗剂。

Exploring the Interaction Mechanism of Desmethyl-broflanilide in Insect GABA Receptors and Screening Potential Antagonists by Simulations.

机构信息

Hubei Key Laboratory of Novel Reactor and Green Chemical Technology, School of Chemical Engineering and Pharmacy, Wuhan Institute of Technology, Wuhan 430205, P. R. China.

Education Ministry Key Laboratory of Integrated Management of Crop Diseases and Pests, College of Plant Protection, Nanjing Agricultural University, Nanjing 210095, P. R. China.

出版信息

J Agric Food Chem. 2020 Dec 16;68(50):14768-14780. doi: 10.1021/acs.jafc.0c05728. Epub 2020 Dec 4.

Abstract

Broflanilide, a novel insecticide, is classified as a negative allosteric modulator (NAM) of insect γ-aminobutyric acid (GABA) receptors (GABARs) as desmethyl-broflanilide (DMBF) allosterically inhibits the GABA-induced responses. The G277M mutation of the GABAR subunit has been reported to abolish the inhibitory activity of DMBF. The binding mode of DMBF in insect GABARs needs to be clarified to understand the underlying mechanism of this mutation and to develop novel, efficient NAMs of insect GABARs. Here, we found that a hydrogen bond formed between DMBF and G277 of the GABAR model might be the key interaction for the antagonism of DMBF by simulations. The volume increase induced by the G277M mutation blocks the entrance of the binding pocket, making it difficult for DMBF to enter the binding pocket and thereby decreasing its activity. The following virtual screening and bioassay results identified a novel NAM candidate of insect GABARs. Overall, we reported a possible binding mode of DMBF in insect GABARs and proposed the insensitivity mechanism of the G277M mutant GABAR to DMBF using molecular simulations. The identified NAM candidates might provide more alternatives or potentials for the design of GABAR-targeting insecticides.

摘要

溴氟虫酰胺是一种新型杀虫剂,被归类为昆虫 γ-氨基丁酸(GABA)受体(GABARs)的负变构调节剂(NAM),因为去甲基溴氟虫酰胺(DMBF)变构抑制 GABA 诱导的反应。已经报道了 GABAR 亚基的 G277M 突变会消除 DMBF 的抑制活性。需要阐明 DMBF 在昆虫 GABARs 中的结合模式,以了解这种突变的潜在机制,并开发新型、有效的昆虫 GABARs 的 NAMs。在这里,我们发现 DMBF 与 GABAR 模型中的 G277 之间形成的氢键可能是通过模拟拮抗 DMBF 的关键相互作用。G277M 突变引起的体积增加会阻碍结合口袋的入口,使 DMBF 难以进入结合口袋,从而降低其活性。随后的虚拟筛选和生物测定结果确定了一种新型的昆虫 GABARs 的 NAM 候选物。总体而言,我们报告了 DMBF 在昆虫 GABARs 中的可能结合模式,并通过分子模拟提出了 G277M 突变 GABAR 对 DMBF 不敏感的机制。鉴定出的 NAM 候选物可能为 GABA 靶向杀虫剂的设计提供更多的替代品或潜力。

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