2007年
Effects of the structures of ecdysone receptor (EcR) and ultraspiracle (USP) on the ligand-binding activity of the EcR/USP heterodimer
JOURNAL OF PESTICIDE SCIENCE
- ,
- ,
- ,
- 巻
- 32
- 号
- 4
- 開始ページ
- 379
- 終了ページ
- 384
- 記述言語
- 英語
- 掲載種別
- 研究論文(学術雑誌)
- DOI
- 10.1584/jpestics.G07-19
- 出版者・発行元
- PESTICIDE SCI SOC JAPAN
N-tert-Butyl-N,N'-diacylhydrazine (DAH) analogs are nonsteroidal ecdysone agonists. The binding activity of DAH analogs to the heterodimer of the ecdysone receptor (EcR) and ultraspiracle (USP) is diverse among insect species, which is probably the main factor causing their selective toxicity. We prepared EcR and USP proteins from lepidopteran Chilo suppressalis, dipteran Drosophila melanogaster and coleopteran Leptinotarsa decemlineata, and measured the binding activity of ecdysone agonists against various hybrid EcR/USP heterodimers. There was a linear relationship between binding activities (pIC(50) values) before and after replacing native USP with that derived from other insects, suggesting that the selective toxicity of DAH analogs is mainly dependent on the EcR structure and not the USP structure. (C) Pesticide Science Society of Japan.
- リンク情報
- ID情報
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- DOI : 10.1584/jpestics.G07-19
- ISSN : 1348-589X
- Web of Science ID : WOS:000252451100004