首页> 外文期刊>FEBS letters. >Mutations in DIIS5 and the DIIS4-S5 linker of Drosophila melanogaster sodium channel define binding domains for pyrethroids and DDT.
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Mutations in DIIS5 and the DIIS4-S5 linker of Drosophila melanogaster sodium channel define binding domains for pyrethroids and DDT.

机译:果蝇钠通道的DIIS5和DIIS4-S5接头中的突变定义了拟除虫菊酯和DDT的结合域。

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摘要

Mutations in the DIIS4-S5 linker and DIIS5 have identified hotspots of pyrethroid and DDT interaction with the Drosophila para sodium channel. Wild-type and mutant channels were expressed in Xenopus oocytes and subjected to voltage-clamp analysis. Substitutions L914I, M918T, L925I, T929I and C933A decreased deltamethrin potency, M918T, L925I and T929I decreased permethrin potency and T929I, L925I and I936V decreased fenfluthrin potency. DDT potency was unaffected by M918T, but abolished by T929I and reduced by L925I, L932F and I936V, suggesting that DIIS5 contains at least part of the DDT binding domain. The data support a computer model of pyrethroid and DDT binding.
机译:DIIS4-S5接头和DIIS5中的突变已确定了拟除虫菊酯和DDT与果蝇对位钠通道相互作用的热点。野生型和突变型通道在非洲爪蟾卵母细胞中表达,并进行电压钳分析。替代品L914I,M918T,L925I,T929I和C933A降低了溴氰菊酯的效力,M918T,L925I和T929I降低了苄氯菊酯的效力,而T929I,L925I和I936V降低了芬氟菊酯的效力。 D918的效力不受M918T的影响,但被T929I废除,而被L925I,L932F和I936V降低,表明DIIS5至少包含DDT结合域的一部分。数据支持拟除虫菊酯和DDT结合的计算机模型。

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