首页> 外文期刊>The Journal of Physiology >Modulation of reconstituted ATP-sensitive K(+)-channels by GTP-binding proteins in a mammalian cell line.
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Modulation of reconstituted ATP-sensitive K(+)-channels by GTP-binding proteins in a mammalian cell line.

机译:重组ATP敏感性K(+)通道的哺乳动物细胞系中的GTP结合蛋白的调制。

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摘要

1. The action of GTP-binding proteins on ATP-sensitive potassium (KATP) channels was investigated. KATP channels were expressed in a mammalian cell line (COS-1 cells) by cotransfecting vectors carrying the sulphonylurea receptor (SUR1) and BIR (Kir6.2), a member of the inward rectifier K+ channel family. G proteins were also tested on KATP channels composed of an isoform of SUR1, SUR2A, in combination with Kir6.2. 2. The alpha and beta gamma subunits of the GTP binding protein G1 were tested separately in inside-out patches under continuous recording. G alpha-11 increases the activity of SUR1-Kir6.2 and SUR2A-Kir6.2 channels by 200 and by 30%, respectively. 3. G alpha-12 does not increase the activity of SUR1-Kir6.2 channels, but increase the activity of SUR2A-Kir6.2 channels by 30%. 4. Control experiments showed that GTP gamma S, a specific activator of G proteins, and heat-inactivated G alpha-11 do not increase the single channel activity. 5. No effects of the other subunits (beta gamma) from either G11 or G12 on the single channel activity were observed. 6. The protein kinase C inhibitors H7 and an inhibitory peptide (FARKGALRQKNV) had no effect on the modulatory action of G alpha-11 on SUR1-Kir6.2 channels. 7. We conclude that both types of reconstituted KATP channels are modulated by G proteins.
机译:1.研究了GTP结合蛋白对ATP敏感性钾(KATP)通道的作用。通过共转染携带磺酰脲受体(SUR1)和BIR(Kir6.2)(内向整流K +通道家族成员)的载体,在哺乳动物细胞系(COS-1细胞)中表达KATP通道。还在由SUR1,SUR2A和Kir6.2的同工型组成的KATP通道上测试了G蛋白。 2.在连续记录下,在由内而外的贴片中分别测试了GTP结合蛋白G1的α和βγ亚基。 G alpha-11将SUR1-Kir6.2和SUR2A-Kir6.2通道的活性分别提高200%和30%。 3. G alpha-12不会增加SUR1-Kir6.2通道的活性,但会使SUR2A-Kir6.2通道的活性增加30%。 4.对照实验显示GTPγS(一种G蛋白的特异性激活剂)和热灭活的G alpha-11不会增加单通道活性。 5.没有观察到来自G11或G12的其他亚基(βγ)对单通道活性的影响。 6.蛋白激酶C抑制剂H7和抑制肽(FARKGALRQKNV)对Gα-11对SUR1-Kir6.2通道的调节作用没有影响。 7.我们得出结论,两种重构的KATP通道均受G蛋白调节。

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