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使用 HEK293T 细胞的蜕皮激素激动剂荧光素酶报告基因检测法。

A luciferase reporter assay for ecdysone agonists using HEK293T cells.

机构信息

Division of Applied Life Sciences, Graduate School of Agriculture, Kyoto University, Kitashirakawa Oiwake-cho, Sakyo-ku, Kyoto, Japan.

Department of RNA Biology and Neuroscience, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita, Osaka, Japan.

出版信息

Biosci Biotechnol Biochem. 2022 Oct 20;86(11):1490-1496. doi: 10.1093/bbb/zbac139.

Abstract

Ecdysone agonists are a class of insecticides that activate the ecdysone receptor (EcR) heterodimerized with the ultraspiracle (USP). Here, we report a new luciferase reporter assay for ecdysone agonists. The assay employs mammalian HEK293T cells transiently transfected with the EcR and USP genes of Chilo suppressalis, along with the taiman (Tai) gene of Drosophila melanogaster that encodes a steroid receptor coactivator. This assay system gave results consistent with those of radioligand binding assays and showed sensitivity superior to that of the existing in vitro methods. In addition, use of the heterologous host cells precludes perturbation from intrinsic players of the ecdysone signaling, which is a potential drawback of insect cell-based methods. This reporter system is suitable for detailed structure-activity analysis of ecdysone agonists and will serve as a valuable tool for the rational design of novel insect growth regulators.

摘要

蜕皮激素激动剂是一类杀虫剂,可激活与超螺旋体(USP)异二聚化的蜕皮激素受体(EcR)。在这里,我们报告了一种新的蜕皮激素激动剂的荧光素酶报告基因检测法。该检测法采用瞬时转染了斜纹夜蛾(Chilo suppressalis)EcR 和 USP 基因以及编码类固醇受体共激活因子的果蝇(Drosophila melanogaster)Tai 基因的哺乳动物 HEK293T 细胞。该检测系统的结果与放射性配体结合检测法的结果一致,并且其灵敏度优于现有的体外方法。此外,使用异源宿主细胞可避免内源性蜕皮激素信号传导参与者的干扰,这是基于昆虫细胞的方法的潜在缺点。该报告基因系统适用于蜕皮激素激动剂的详细结构-活性分析,并且将成为新型昆虫生长调节剂的合理设计的有价值工具。

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