The impermeant ion methylammonium blocks K+ and NH4+ currents through KAT1 channel differently:: Evidence for ion interaction in channel permeation

被引:22
作者
Moroni, A
Bardella, L
Thiel, G
机构
[1] Univ Milan, Dipartimento Fisiol & Biochim Gen, Sez Fisiol Gen, Lab Elettrofisiol, I-20133 Milan, Italy
[2] Univ Milan, Dipartimento Fisiol & Biochim Gen, Sez Patol Gen, I-20133 Milan, Italy
[3] Univ Gottingen, Inst Plant Physiol, D-37073 Gottingen, Germany
关键词
KAT1; potassium channel; permeation; block; ammonium (NH4+); methylammonium (MA);
D O I
10.1007/s002329900367
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 permeation properties of KAT1, an inward rectifying potassium channel from plant cells, were investigated with different ions in the external medium. With either K+, NH4+ or methylammonium (MA) in the external solution, the channel, expressed in Xenopus oocytes, appeared permeable to K+ and, to a lesser extent, to NH4+ but not to the slightly bigger, methylated analogue of NH4+, MA. Substituting NH4+ for K+ shifted the voltage dependency of channel activation further negative and hastened activation kinetics. This suggests that channel operation depends on the transported substrate. In mixed solution (50 mM K+, 50 mM MA) MA inhibited K+ current in a voltage-independent manner. The maximum block did not exceed 50% of the K+ current. In contrast, when NH4+ was the permeant ion (50 mM NH4+, 50 mM MA) MA caused a voltage-dependent, slowly developing open channel block, achieving complete inhibition at very negative voltages. The latter block could be partially overcome by the addition of K+ in the external solution. The data support a model in which ions, after entering the channel pore, compete with different affinities for binding sites on their permeation pathway.
引用
收藏
页码:25 / 35
页数:11
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