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A distinct sodium channel voltage-sensor locus determines insect selectivity of the spider toxin Dc1a

机译:独特的钠通道电压传感器位点决定了蜘蛛毒素Dc1a的昆虫选择性

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摘要

β-Diguetoxin-Dc1a (Dc1a) is a toxin from the desert bush spider Diguetia canities that incapacitates insects at concentrations that are non-toxic to mammals. Dc1a promotes opening of German cockroach voltage-gated sodium (Nav) channels (BgNav1), whereas human Nav channels are insensitive. Here, by transplanting commonly targeted S3b-S4 paddle motifs within BgNav1 voltage sensors into Kv2.1, we find that Dc1a interacts with the domain II voltage sensor. In contrast, Dc1a has little effect on sodium currents mediated by PaNav1 channels from the American cockroach even though their domain II paddle motifs are identical. When exploring regions responsible for PaNav1 resistance to Dc1a, we identified two residues within the BgNav1 domain II S1–S2 loop that when mutated to their PaNav1 counterparts drastically reduce toxin susceptibility. Overall, our results reveal a distinct region within insect Nav channels that helps determine Dc1a sensitivity, aconcept that will be valuable for the design of insect-selective insecticides.
机译:β-Diguetoxin-Dc1a(Dc1a)是沙漠灌木蜘蛛Diguetia罐头中的一种毒素,能以对哺乳动物无毒的浓度使昆虫失能。 Dc1a促进打开德国蟑螂电压门控钠(Nav)通道(BgNav1),而人类Nav通道不敏感。在这里,通过将BgNav1电压传感器内的通用目标S3b-S4桨状图案移植到Kv2.1,我们发现Dc1a与域II电压传感器相互作用。相比之下,Dc1a对美国蟑螂的PaNav1通道介导的钠电流影响很小,即使它们的结构域II桨基序相同。当探索负责PaNav1对Dc1a抗性的区域时,我们在BgNav1域II S1-S2环中发现了两个残基,当它们突变为PaNav1对应物时,它们会极大地降低毒素的敏感性。总的来说,我们的研究结果揭示了昆虫Nav通道内的一个独特区域,该区域有助于确定Dc1a敏感性,这一概念对于设计昆虫选择性杀虫剂具有重要意义。

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