Tucker S J, Gribble F M, Proks P, Trapp S, Ryder T J, Haug T, Reimann F, Ashcroft F M
University Laboratory of Physiology, Oxford OX1 3PT, UK.
EMBO J. 1998 Jun 15;17(12):3290-6. doi: 10.1093/emboj/17.12.3290.
ATP-sensitive K+ (KATP) channels are both inhibited and activated by intracellular nucleotides, such as ATP and ADP. The inhibitory effects of nucleotides are mediated via the pore-forming subunit, Kir6.2, whereas the potentiatory effects are conferred by the sulfonylurea receptor subunit, SUR. The stimulatory action of Mg-nucleotides complicates analysis of nucleotide inhibition of Kir6. 2/SUR1 channels. We therefore used a truncated isoform of Kir6.2, that expresses ATP-sensitive channels in the absence of SUR1, to explore the mechanism of nucleotide inhibition. We found that Kir6.2 is highly selective for ATP, and that both the adenine moiety and the beta-phosphate contribute to specificity. We also identified several mutations that significantly reduce ATP inhibition. These are located in two distinct regions of Kir6.2: the N-terminus preceding, and the C-terminus immediately following, the transmembrane domains. Some mutations in the C-terminus also markedly increased the channel open probability, which may account for the decrease in apparent ATP sensitivity. Other mutations did not affect the single-channel kinetics, and may reduce ATP inhibition by interfering with ATP binding and/or the link between ATP binding and pore closure. Our results also implicate the proximal C-terminus in KATP channel gating.
ATP敏感性钾离子(KATP)通道受细胞内核苷酸如ATP和ADP的抑制与激活。核苷酸的抑制作用通过成孔亚基Kir6.2介导,而增强作用则由磺脲类受体亚基SUR赋予。镁核苷酸的刺激作用使对Kir6.2/SUR1通道核苷酸抑制作用的分析变得复杂。因此,我们使用了Kir6.2的截短异构体,其在没有SUR1的情况下表达ATP敏感性通道,以探究核苷酸抑制的机制。我们发现Kir6.2对ATP具有高度选择性,腺嘌呤部分和β-磷酸都对特异性有贡献。我们还鉴定了几个显著降低ATP抑制作用的突变。这些突变位于Kir6.2的两个不同区域:跨膜结构域之前的N端和紧随其后的C端。C端的一些突变也显著增加了通道开放概率,这可能解释了表观ATP敏感性的降低。其他突变不影响单通道动力学,可能通过干扰ATP结合和/或ATP结合与孔道关闭之间的联系来降低ATP抑制作用。我们的结果还表明近C端参与了KATP通道门控。