Voltage-dependent inhibition of the Na+,K+ pump by tetraethylammonium

被引:18
作者
Eckstein-Ludwig, U
Rettinger, J
Vasilets, LA
Schwarz, W
机构
[1] Max Planck Inst Biophys, D-60596 Frankfurt, Germany
[2] Univ Frankfurt, Biozentrum, Inst Pharmakol, D-60439 Frankfurt, Germany
[3] Russian Acad Sci, Inst Chem Phys, Chernogolovka 142432, Moscow Region, Russia
来源
BIOCHIMICA ET BIOPHYSICA ACTA-BIOMEMBRANES | 1998年 / 1372卷 / 02期
关键词
TEA; Na+; K+-ATPase; oocyte; pump current; ouabain; (Xenopus);
D O I
10.1016/S0005-2736(98)00066-2
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
Tetraethylammonium (TEA(+)) is an effective inhibitor of a variety of K+-channels, and has been widely used to reduce K+-sensitive background conductances in electrophysiological investigations of the Na+,K+-ATPase. Here we demonstrate by combination of two-electrode voltage clamp (TEVC) and giant patch clamp of Xenopus oocytes, and measurements of the activity of purified ATPase of pig kidney that TEA(+) directly inhibits the Na+,K+-ATPase from the outside. The K-I value in TEVC experiments at 0 mV is about 10 mM increasing with more negative potentials. A similar voltage-dependent inhibition by TEA(+) was observed in the excised membrane patches except that the apparent K-I value at 0 mV is about 100 mM, a value nearly identical to that found for inhibition of purified kidney ATPase. The voltage-dependent inhibition can be described by an effective valency of 0.39 and is attributed to an interference with the voltage-dependent binding of K+ at an external access channel. The apparent dielectric length of the access channel for K+ is not affected by TEA(+). (C) 1998 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:289 / 300
页数:12
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