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Ligand-Dependent Effects on the Conformational Equilibrium of the Na+,K+-ATPase As Monitored by Voltage Clamp Fluorometry

机译:电压钳荧光法监测的Na +,K + -ATPase构象平衡的配体依赖性效应

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摘要

Voltage clamp fluorometry was used to monitor conformational changes associated with electrogenic partial reactions of the Na+,K+-ATPase after changes in the concentration of internal sodium (Na+i) or external potassium (K+o). To probe the effects of the Na+i concentration on the Na+ branch of the Na+,K+-ATPase, oocytes were depleted of Na+i and then loaded with external sodium (Na+o) using the amiloride-sensitive epithelial sodium channel. The K+ branch of the Na+,K+-ATPase was studied by exposing the oocytes to different K+o concentrations in the presence and absence of Na+o to obtain additional information on the apparent affinity for K+o. Our results demonstrate that lowering the concentration of Na+i or increasing the amount of K+o in the external solution shifts the equilibrium toward E1/E1P. Furthermore, the K+o-induced relocation toward E1 occurs at a much lower K+o concentration when Na+o is absent, indicating a higher apparent affinity. Finally, voltage-dependent steps associated with the K+ branch or the Na+ branch of the Na+,K+-ATPase are affected by the K+o concentration or the Na+i concentration, respectively.
机译:在内部钠(Na + i)或外部钾(K + o)浓度变化后,电压钳荧光法用于监测与Na +,K + -ATPase的电部分反应相关的构象变化。为了探测Na + i浓度对Na +,K + -ATPase的Na +分支的影响,将卵母细胞中的Na + i消耗掉,然后使用阿米洛利敏感的上皮钠通道向其添加外部钠(Na + o)。通过在有和没有Na + o的情况下将卵母细胞暴露于不同的K + o浓度来研究Na +,K + -ATPase的K +分支,以获得有关对K + o的表观亲和力的其他信息。我们的结果表明,降低Na + i的浓度或增加外部溶液中K + o的量会使平衡向E1 / E1P移动。此外,当不存在Na + o时,K + o诱导的向E1的重定位以低得多的K + o浓度发生,表明较高的表观亲和力。最后,与Na +,K + -ATP酶的K +分支或Na +分支相关的电压依赖性步骤分别受K + o浓度或Na + i浓度影响。

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