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Gating of Cyclic Nucleotide-Gated (CNGA1) Channels by cGMP Jumps and Depolarizing Voltage Steps

机译:通过cGMP跳跃和去极化电压阶跃对环核苷酸门控(CNGA1)通道进行门控

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摘要

We expressed rod-type homotetrameric cyclic nucleotide-gated (CNGA1) channels in Xenopus oocytes and studied activation by photolysis-induced jumps of the 3′,5′-cyclic guanosine monophosphate (cGMP) concentration and by voltage steps. cGMP jumps to increasing concentrations up to the EC50 value of 46.5 μM decelerate the activation gating, indicative that even at concentrations of cGMP ≪EC50 binding is not rate limiting. Above the EC50 value, activation by cGMP jumps is again accelerated to the higher concentrations. At the same cGMP concentration, the speed of the activation gating by depolarizing voltage steps is roughly similar to that by cGMP jumps. Permeating ions passing the pore more slowly (Rb+ > K+ > Na+) slow down the activation time course. At the single-channel level, cGMP jumps to high concentrations cause openings directly to the main open level without passing sublevels. From these results it is concluded that at both low and high cGMP the gating of homotetrameric CNGA1 channels is not rate-limited by the cGMP binding but by conformational changes of the channel which are voltage dependent and include movements in the pore region.
机译:我们在非洲爪蟾卵母细胞中表达杆型同四聚体环状核苷酸门控(CNGA1)通道,并通过光解诱导的3',5'-环鸟苷单磷酸(cGMP)浓度的跃迁和电压阶跃研究了激活。 cGMP跃升至浓度增加,直至EC50值达到46.5μM,使激活门控减速,这表明即使在cGMP ≪EC50浓度下,结合也不是速率限制。高于EC50值,cGMP跳跃激活再次被加速到更高的浓度。在相同cGMP浓度下,通过使电压阶跃去极化来激活门控的速度与通过cGMP跳跃实现的门控速度大致相似。渗透离子通过孔的速度更慢(Rb + + + )会减慢激活时间。在单通道级别上,cGMP跳到很高的浓度,导致直接打开到主打开级别而没有通过子级别。从这些结果可以得出结论,在低cGMP和高cGMP时,同四聚体CNGA1通道的门控均不受cGMP结合的速率限制,但受通道的构象变化的限制,该构象变化取决于电压并包括孔区域的运动。

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