Du Yuzhe, Nomura Yoshiko, Zhorov Boris S, Dong Ke
Department of Entomology, Genetics, and Neuroscience Programs, Michigan State University, East Lansing, Michigan (Y.D., Y.N., K.D.); Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada (B.S.Z.); and Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St. Petersburg, Russia (B.S.Z.).
Department of Entomology, Genetics, and Neuroscience Programs, Michigan State University, East Lansing, Michigan (Y.D., Y.N., K.D.); Department of Biochemistry and Biomedical Sciences, McMaster University, Hamilton, Ontario, Canada (B.S.Z.); and Sechenov Institute of Evolutionary Physiology and Biochemistry, Russian Academy of Sciences, St. Petersburg, Russia (B.S.Z.)
Mol Pharmacol. 2015 Aug;88(2):273-80. doi: 10.1124/mol.115.098707. Epub 2015 May 13.
Voltage-gated sodium channels are the primary target of pyrethroid insecticides. Although it is well known that specific mutations in insect sodium channels confer knockdown resistance (kdr) to pyrethroids, the atomic mechanisms of pyrethroid-sodium channel interactions are not clearly understood. Previously, computer modeling and mutational analysis predicted two pyrethroid receptors, pyrethroid receptor site 1 (PyR1) (initial) and pyrethroid receptor site 2 (PyR2), located in the domain interfaces II/III and I/II, respectively. The models differ in ligand orientation and the number of transmembrane helices involved. In this study, we elaborated a revised PyR1 model of the mosquito sodium channel. Computational docking in the Kv1.2-based open channel model yielded a complex in which a pyrethroid (deltamethrin) binds between the linker helix IIL45 and transmembrane helices IIS5, IIS6, and IIIS6 with its dibromoethenyl and diphenylether moieties oriented in the intra- and extracellular directions, respectively. The PyR2 and revised PyR1 models explained recently discovered kdr mutations and predicted new deltamethrin-channel contacts. Further model-driven mutagenesis identified seven new pyrethroid-sensing residues, three in the revised PyR1 and four in PyR2. Our data support the following conclusions: 1) each pyrethroid receptor is formed by a linker-helix L45 and three transmembrane helices (S5 and two S6s); 2) IIS6 contains four residues that contribute to PyR1 and another four to PyR2; 3) seven pairs of pyrethroid-sensing residues are located in symmetric positions within PyR1 and PyR2; and 4) pyrethroids bind to PyR1 and PyR2 in similar orientations, penetrating deeply into the respective domain interfaces. Our study elaborates the dual pyrethroid-receptor sites concept and provides a structural background for rational development of new insecticides.
电压门控钠通道是拟除虫菊酯类杀虫剂的主要作用靶点。虽然已知昆虫钠通道中的特定突变会赋予对拟除虫菊酯的击倒抗性(kdr),但拟除虫菊酯与钠通道相互作用的原子机制尚不清楚。此前,计算机建模和突变分析预测了两个拟除虫菊酯受体,分别是位于结构域界面II/III和I/II的拟除虫菊酯受体位点1(PyR1)(初始)和拟除虫菊酯受体位点2(PyR2)。这些模型在配体方向和涉及的跨膜螺旋数量上有所不同。在本研究中,我们精心构建了一个修订后的蚊子钠通道PyR1模型。基于Kv1.2的开放通道模型中的计算对接产生了一个复合物,其中一种拟除虫菊酯(溴氰菊酯)结合在连接螺旋IIL45与跨膜螺旋IIS5、IIS6和IIIS6之间,其二溴乙烯基和二苯醚部分分别朝向细胞内和细胞外方向。PyR2和修订后的PyR1模型解释了最近发现的kdr突变,并预测了新的溴氰菊酯与通道的接触点。进一步的模型驱动诱变鉴定出七个新的拟除虫菊酯感应残基,其中三个在修订后的PyR1中,四个在PyR2中。我们的数据支持以下结论:1)每个拟除虫菊酯受体由一个连接螺旋L45和三个跨膜螺旋(S5和两个S6)组成;2)IIS6包含四个对PyR1有贡献的残基和另外四个对PyR2有贡献的残基;3)七对拟除虫菊酯感应残基位于PyR1和PyR2内的对称位置;4)拟除虫菊酯以相似的方向与PyR1和PyR2结合,深入穿透各自的结构域界面。我们的研究阐述了双拟除虫菊酯受体位点的概念,并为合理开发新型杀虫剂提供了结构背景。