Electrostatic interactions in the channel cavity as an important determinant of potassium channel selectivity

被引:32
作者
Bichet, Delphine
Grabe, Michael
Jan, Yuh Nung
Jan, Lily Yeh [1 ]
机构
[1] Univ Calif San Francisco, Dept Physiol & Biochem, San Francisco, CA 94143 USA
[2] Univ Calif San Francisco, Howard Hughes Med Inst, San Francisco, CA 94143 USA
关键词
inward rectification; permeation; permeability; GIRK modeling; Kir3;
D O I
10.1073/pnas.0606660103
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Potassium channels are membrane proteins that allow the passage of potassium ions at near diffusion rates while severely limiting the flux of the slightly smaller sodium ions. Although studies thus far have focused on the narrowest part of the channel, known as the selectivity filter, channels are long pores with multiple ions that traverse the selectivity filter, the water-filled central cavity, and the rest of the pore formed by cytoplasmic domains. Here, we present experimental analyses on Kir3.2 (GIRK2), a G protein-activated inwardly rectifying potassium (Kir) channel, showing that a negative charge introduced at a pore-facing position in the cavity (N184) below the selectivity filter restores both K+ selectivity and inward rectification properties to the nonselective S177W mutant channel. Molecular modeling demonstrates that the negative residue has no effect on the geometry of the selectivity filter, suggesting that it has a local effect on the cavity ion. Moreover, restoration of selectivity does not depend on the exact location of the charge in the central cavity as long as this residue faces the pore, where it is in close contact with permeant ions. Our results indicate that interactions between permeant ions and the channel cavity can influence ion selectivity and channel block by means of an electrostatic effect.
引用
收藏
页码:14355 / 14360
页数:6
相关论文
共 39 条
[1]  
Ashcroft F.M., 2000, Ion Channels and Disease
[2]  
Bhattacharjee A, 2003, J NEUROSCI, V23, P11681
[3]   Evolving potassium channels by means of yeast selection reveals structural elements important for selectivity [J].
Bichet, D ;
Lin, YF ;
Ibarra, CA ;
Huang, CS ;
Yi, BA ;
Jan, YN ;
Jan, LY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (13) :4441-4446
[4]   Merging functional studies with structures of inward-rectifier K+ channels [J].
Bichet, D ;
Haass, FA ;
Jan, LY .
NATURE REVIEWS NEUROSCIENCE, 2003, 4 (12) :957-967
[5]   Plant K+ transport:: Not just an uphill struggle [J].
Brownlee, C .
CURRENT BIOLOGY, 2002, 12 (11) :R402-R404
[6]   The pore helix dipole has a minor role in inward rectifier channel function [J].
Chatelain, FC ;
Alagem, N ;
Xu, Q ;
Pancaroglu, R ;
Reuveny, E ;
Minor, DL .
NEURON, 2005, 47 (06) :833-843
[7]   Permeation properties of inward-rectifier potassium channels and their molecular determinants [J].
Choe, H ;
Sackin, H ;
Palmer, LG .
JOURNAL OF GENERAL PHYSIOLOGY, 2000, 115 (04) :391-404
[8]   Molecular basis of ion selectivity, block, and rectification of the inward rectifier Kir3.1/Kir3.4 K+ channel [J].
Dibb, KM ;
Rose, T ;
Makary, SY ;
Claydon, TW ;
Enkvetchakul, D ;
Leach, R ;
Nichols, CG ;
Boyett, MR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (49) :49537-49548
[9]   The structure of the potassium channel:: Molecular basis of K+ conduction and selectivity [J].
Doyle, DA ;
Cabral, JM ;
Pfuetzner, RA ;
Kuo, AL ;
Gulbis, JM ;
Cohen, SL ;
Chait, BT ;
MacKinnon, R .
SCIENCE, 1998, 280 (5360) :69-77
[10]   Ser165 in the second transmembrane region of the Kir2.1 channel determines its susceptibility to blockade by intracellular Mg2+ [J].
Fujiwara, Y ;
Kubo, Y .
JOURNAL OF GENERAL PHYSIOLOGY, 2002, 120 (05) :677-692