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IPPA08 allosterically enhances the action of imidacloprid on nicotinic acetylcholine receptors

文献类型： 外文期刊

作者： Bao, Haibo 1 ; Shao, Xusheng 3 ; Zhang, Yixi 2 ; Cheng, Jiagao; Wang, Yunchao 2 ; Xu, Xiaoyong; Fang, Jichao 1 ; Li 1 ;

作者机构： 1.Jiangsu Acad Agr Sci, Inst Plant Protect, St Zhongling 50, Nanjing 210014, Jiangsu, Peoples R China

2.Nanjing Agr Univ, Coll Plant Protect, Key Lab Integrated Management Crop Dis & Pests, Minist Educ, Weigang 1, Nanjing 210095, Jiangsu, Peoples R China

3.East China Univ Sci & Technol, Shanghai Key Lab Chem Biol, Sch Pharm, Meilong Rd 130, Shanghai 200237, Peoples R China

4.East China Univ Sci & Technol, Shanghai Key Lab Chem Biol, Sch Pharm, Meilong Rd 130, Shanghai

关键词： Nicotinic acetylcholine receptors;IPPA08;Synergistic mechanism;Noncanonical interface

期刊名称：INSECT BIOCHEMISTRY AND MOLECULAR BIOLOGY （ 影响因子：4.714； 五年影响因子：4.953 ）

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收录情况： SCI

摘要： Our previous study showed that IPPA08, a cis-configuration neonicotinoid compound with unique oxabridged substructure, acted as a specific synergist to neonicotinoid insecticides targeting nicotinic acetylcholine receptors (nAChRs). Heteropentamer nAChRs have diverse characteristics and can form canonical and noncanonical subunit interfaces. While canonical interfaces have been exploited as targets of many drugs, noncanonical interfaces have received less attention. In this study, the mechanism of IPPA08 synergism was evaluated on hybrid nAChRs consisting of three alpha 1 subunits from the brown planthopper and two rat beta 1 subunits (Nl alpha 1/r beta 2) expressed in Xenopus oocytes. IPPA08 alone evoked inward currents, but only at very high concentrations, greater than 1 mM. However, at concentrations below 200 mu M, IPPA08 slowed the decay of inward currents evoked by imidacloprid, but not by acetylcholine, and also increased the sensitivity of Nl alpha 1/r beta 2 to imidacloprid. Both modulations by IPPA08 were concentration-dependent in the same concentration range of 10-150 mu M. Experimentally induced mutations in canonical (alpha+/beta-) and noncanonical (beta+/alpha-) interfaces of NI alpha 1/r beta 2 receptors were also examined to evaluate the presence of possible binding sites for IPPA08 on the receptors. Our results showed that mutations in the canonical interfaces affected only the potency of IPPA08 as an agonist, while mutations in the noncanonical interfaces affected only the synergistic action of IPPA08. Based on these results, we propose that at low concentrations IPPA08 can act as a positive allosteric modulator of noncanonical interfaces, and likely slow the decay of currents through stabilizing the open-channel state caused by the action of imidacloprid on canonical interfaces. (C) 2016 Elsevier Ltd. All rights reserved.

  • 相关文献

[1]Selective actions of Lynx proteins on different nicotinic acetylcholine receptors in the locust, Locusta migratoria manilensis. Wang, Xin,Bao, Haibo,Sun, Huahua,Zhang, Yixi,Liu, Qinghong,Liu, Zewen,Bao, Haibo,Fang, Jichao.

[2]Two distinctive beta subunits are separately involved in two binding sites of imidacloprid with different affinities in Locusta migratoria manilensis. Bao, Haibo,Liu, Yang,Zhang, Yixi,Liu, Zewen,Bao, Haibo. 2017

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