首页> 外文会议>Pan-Pacific Conference on Pesticide Science >Measurement of Receptor-Binding Activity of Non-Steroidal Ecdysone Agonists Using in vitro Expressed Receptor Proteins (EcR/USP Complex) of Chilo suppressalis and Drosophila melanogaster
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Measurement of Receptor-Binding Activity of Non-Steroidal Ecdysone Agonists Using in vitro Expressed Receptor Proteins (EcR/USP Complex) of Chilo suppressalis and Drosophila melanogaster

机译:使用体外表达受体蛋白(ECR / USP复合物)的非甾体蜕皮酶激动剂的受体结合活性的测量嗜睡抑制和果蝇黑素蛋白酶

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N-tert-Butyl-N,N'-dibenzoylhydrazine and its analogs are agonists of insect molting hormone (20-hydroxyecdysone: 20E). In order to elucidate the mode of action of these non-steroidal ecdysone agonists at the molecular level, we expressed the receptor protein for 20E - the heterodimer of ecdysone receptor (EcR) and ultraspiracle (USP) - in vitro, and analyzed their binding affinities to ligands. For the lepidopteran Chilo suppressalis, we showed quantitatively that the receptor-binding activity of non-steroidal ecdysone agonists determines the strength of their molting hormonal and insecticidal activities. The binding activity of five representative non-steroidal ecdysone agonists to C. suppressalis EcR/USP was higher than that to dipteran Drosophila melanogaster EcR/USP, which probably results in the selective toxicity between these two insects.
机译:N-叔丁基-N,N'-二苯甲酰肼及其类似物是昆虫蜕皮激素的激动剂(20-羟基粥样酮:20e)。为了阐明这些非甾体蜕膜激动剂在分子水平下的作用方式,我们表达了20E的受体蛋白 - 体外蜕皮受体(ECR)和超自眼(USP) - 体外的异二聚体,并分析了它们的结合亲和力与配体。对于Lepidopteran Chilo抑制,我们定量表现出非甾体蜕皮蜕膜激动剂的受体结合活性决定了它们蜕变激素和杀虫活性的强度。五个代表性非甾体蜕皮型激动剂至C.抑制的结合活性为C.抑制ECR / USP高于Dipteran Drosophila melanogaster ECR / USP,这可能导致这两种昆虫之间的选择性毒性。

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