Kinetic contribution to extracellular Na+/K+ selectivity in the Na+/K+ pump

被引:2
|
作者
Vleeskens, Elizabeth [1 ]
Clarke, Ronald J. [1 ,2 ]
机构
[1] Univ Sydney, Sch Chem, Sydney, NSW 2006, Australia
[2] Univ Sydney, Nano Inst, Sydney, NSW, Australia
来源
FEBS OPEN BIO | 2018年 / 8卷 / 05期
基金
澳大利亚研究理事会;
关键词
ion selectivity; kinetic modelling; Na+; K+-ATPase; CRYSTAL-STRUCTURE; SODIUM; NA+; K+-ATPASE; TRANSPORT; DEPHOSPHORYLATION; PHOSPHORYLATION;
D O I
10.1002/2211-5463.12418
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The sodium potassium pump (Na+,K+-ATPase) shows a high selectivity for K+ over Na+ binding from the extracellular medium. To understand the K+ selectivity in the presence of a high concentration of competing Na+ ions requires consideration of more than just ion binding affinities. Here, equilibrium-based calculations of the extracellular occupation of the Na+,K+-ATPase transport sites by Na+ and K+ are compared to fluxes through Na+ and K+ transport pathways. The results show that, under physiological conditions, there is a 332-fold selectivity for pumping of K+ from the extracellular medium into the cytoplasm relative to Na+, whereas equilibrium calculations alone predict only a 7.5-fold selectivity for K+. Thus, kinetic effects make a major contribution to the determination of extracellular K+ selectivity.
引用
收藏
页码:854 / 859
页数:6
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