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C型失活控制非洲爪蟾卵母细胞中表达的快速失活心脏钾离子通道(Kv1.4)的恢复。

C-type inactivation controls recovery in a fast inactivating cardiac K+ channel (Kv1.4) expressed in Xenopus oocytes.

作者信息

Rasmusson R L, Morales M J, Castellino R C, Zhang Y, Campbell D L, Strauss H C

机构信息

Department of Biomedical Engineering, Duke University, Durham, NC 27710, USA.

出版信息

J Physiol. 1995 Dec 15;489 ( Pt 3)(Pt 3):709-21. doi: 10.1113/jphysiol.1995.sp021085.

Abstract
  1. A fast inactivating transient K+ current (FK1) cloned from ferret ventricle and expressed in Xenopus oocytes was studied using the two-electrode voltage clamp technique. Removal of the NH2-terminal domain of FK1 (FK1 delta 2-146) removed fast inactivation consistent with previous findings in Kv1.4 channels. The NH2-terminal deletion mutation revealed a slow inactivation process, which matches the criteria for C-type inactivation described for Shaker B channels. 2. Inactivation of FK1 delta 2-146 at depolarized potentials was well described by a single exponential process with a voltage-insensitive time constant. In the range -90 to +20 mV, steady-state C-type inactivation was well described by a Boltzmann relationship that compares closely with inactivation measured in the presence of the NH2-terminus. These results suggest that C-type inactivation is coupled to activation. 3. The coupling of C-type inactivation to activation was assessed by mutation of the fourth positively charged residue (arginine 454) in the S4 voltage sensor to glutamine (R454Q). This mutation produced a hyperpolarizing shift in the inactivation relationship of both FK1 and FK1 delta 2-146 without altering the rate of inactivation of either clone. 4. The rates of recovery from inactivation are nearly identical in FK1 and FK1 delta 2-146. 5. To assess the mechanisms underlying recovery from inactivation the effects of elevated [K+]o and selective mutations in the extracellular pore and the S4 voltage sensor were compared in FK1 and FK1 delta 2-146. The similarity in recovery rates in response to these perturbations suggests that recovery from C-type inactivation governs the overall rate of recovery of inactivated channels for both FK1 and FK1 delta 2-146. 6. Analysis of the rate of recovery of FK1 channels for inactivating pulses of different durations (70-2000 ms) indicates that recovery rate is insensitive to the duration of the inactivating pulse.
摘要
  1. 利用双电极电压钳技术研究了从雪貂心室克隆并在非洲爪蟾卵母细胞中表达的快速失活瞬时钾电流(FK1)。去除FK1的NH2末端结构域(FK1δ2 - 146)后,快速失活现象消失,这与之前在Kv1.4通道中的发现一致。NH2末端缺失突变揭示了一个缓慢失活过程,该过程符合对Shaker B通道描述的C型失活标准。2. FK1δ2 - 146在去极化电位下的失活可用具有电压不敏感时间常数的单指数过程很好地描述。在 - 90至 + 20 mV范围内,稳态C型失活可用玻尔兹曼关系很好地描述,该关系与在存在NH2末端时测得的失活情况密切相关。这些结果表明C型失活与激活相关联。3. 通过将S4电压传感器中第四个带正电荷的残基(精氨酸454)突变为谷氨酰胺(R454Q)来评估C型失活与激活的关联。该突变使FK1和FK1δ2 - 146的失活关系发生超极化偏移,而不改变任何一个克隆的失活速率。4. FK1和FK1δ2 - 146从失活中恢复的速率几乎相同。5. 为了评估从失活中恢复的潜在机制,比较了FK1和FK1δ2 - 146中升高的[K + ]o以及细胞外孔和S4电压传感器中的选择性突变的影响。对这些扰动的恢复速率相似性表明,从C型失活中恢复决定了FK1和FK1δ2 - 146失活通道的总体恢复速率。6. 对不同持续时间(70 - 2000 ms)的失活脉冲的FK1通道恢复速率分析表明,恢复速率对失活脉冲的持续时间不敏感。

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