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利用杆状病毒在昆虫细胞中表达功能活性ATP敏感性钾通道

Expression of functionally active ATP-sensitive K-channels in insect cells using baculovirus.

作者信息

Mikhailov M V, Proks P, Ashcroft F M, Ashcroft S J

机构信息

Nuffield Dept. of Clinical Biochemistry, John Radcliffe Hospital, Headington, Oxford, UK.

出版信息

FEBS Lett. 1998 Jun 16;429(3):390-4. doi: 10.1016/s0014-5793(98)00640-1.

Abstract

We have expressed active ATP-sensitive K-channels (K(ATP) channels) in Spodoptera frugiperda (Sf9) cells using a baculovirus vector. A high yield of active channels was obtained on co-infection with SUR1 and Kir6.2 engineered to contain N- and/or C-terminal tags to permit detection by Western blotting. Channel activity was sensitive to ATP, glibenclamide and diazoxide. Channel activity was also obtained on expression of a C-terminally truncated Kir6.2 (Kir6.2 deltaC26): these channels were blocked by ATP but were insensitive to sulphonylureas. In contrast to Xenopus oocytes and mammalian cells the full length Kir6.2 also gave rise to active channels in Sf9 cells when expressed alone. The highest yield of active K(ATP) channels was obtained on infection with a fusion protein containing SUR1 linked to Kir6.2 deltaC26 via a 6-amino acid linker.

摘要

我们利用杆状病毒载体在草地贪夜蛾(Sf9)细胞中表达了活性ATP敏感性钾通道(K(ATP)通道)。与经过工程改造以包含N端和/或C端标签从而允许通过蛋白质免疫印迹法进行检测的SUR1和Kir6.2共感染时,获得了高产率的活性通道。通道活性对ATP、格列本脲和二氮嗪敏感。在表达C端截短的Kir6.2(Kir6.2 deltaC26)时也获得了通道活性:这些通道被ATP阻断,但对磺酰脲类不敏感。与非洲爪蟾卵母细胞和哺乳动物细胞不同,全长Kir6.2单独表达时在Sf9细胞中也能产生活性通道。在用含有通过6个氨基酸接头与Kir6.2 deltaC26连接的SUR1的融合蛋白感染时,获得了最高产率的活性K(ATP)通道。

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