Physical determinants of strong voltage sensitivity of K+ channel block

被引:29
作者
Xu, Yanping [1 ]
Shin, Hyeon-Gyu [1 ]
Szep, Szilvia [1 ]
Lu, Zhe [1 ]
机构
[1] Univ Penn, Howard Hughes Med Inst, Dept Physiol, Philadelphia, PA 19104 USA
基金
美国国家卫生研究院;
关键词
INWARD-RECTIFIER; POTASSIUM CHANNEL; BINDING-SITE; ANOMALOUS RECTIFICATION; TETRAETHYLAMMONIUM ION; FUNCTIONAL EXPRESSION; CRYSTAL-STRUCTURE; STRUCTURAL BASIS; RECEPTOR-SITE; TEA BLOCKADE;
D O I
10.1038/nsmb.1717
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
Strong voltage sensitivity of inward-rectifier K+ (Kir) channels has been hypothesized to arise primarily from an intracellular blocker displacing up to five K+ ions from the wide, intracellular part of the ion conduction pore outwardly across the narrow ion- selectivity filter. The validity of this hypothesis depends on two assumptions: (i) that five ion sites are located intracellular to the filter and (ii) that the blocker can force essentially unidirectional K+ movement in a pore region generally wider than the combined dimensions of the blocker plus a K+ ion. Here we present a crystal structure of the cytoplasmic portion of a Kir channel with five ions bound and demonstrate that a constriction near the intracellular end of the pore, acting as a gasket, prevents K+ ions from bypassing the blocker. This heretofore unrecognized 'gasket' ensures that the blocker can effectively displace K+ ions across the selectivity filter to generate exceedingly strong voltage sensitivity.
引用
收藏
页码:1252 / U67
页数:8
相关论文
共 59 条
[1]   A cation-π interaction between extracellular TEA and an aromatic residue in potassium channels [J].
Ahern, Christopher A. ;
Eastwood, Amy L. ;
Lester, Henry A. ;
Dougherty, Dennis A. ;
Horn, Richard .
JOURNAL OF GENERAL PHYSIOLOGY, 2006, 128 (06) :649-657
[3]   THE CCP4 SUITE - PROGRAMS FOR PROTEIN CRYSTALLOGRAPHY [J].
BAILEY, S .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1994, 50 :760-763
[4]   SIDE-CHAIN MOTION WITH 2 DEGREES OF FREEDOM IN PEPTIDES - AN NMR-STUDY OF PHENYLALANINE SIDE-CHAINS IN ANTAMANIDE [J].
BREMI, T ;
ERNST, M ;
ERNST, RR .
JOURNAL OF PHYSICAL CHEMISTRY, 1994, 98 (37) :9322-9334
[5]   Crystallography & NMR system:: A new software suite for macromolecular structure determination [J].
Brunger, AT ;
Adams, PD ;
Clore, GM ;
DeLano, WL ;
Gros, P ;
Grosse-Kunstleve, RW ;
Jiang, JS ;
Kuszewski, J ;
Nilges, M ;
Pannu, NS ;
Read, RJ ;
Rice, LM ;
Simonson, T ;
Warren, GL .
ACTA CRYSTALLOGRAPHICA SECTION D-BIOLOGICAL CRYSTALLOGRAPHY, 1998, 54 :905-921
[6]   AMINO-AROMATIC INTERACTIONS IN PROTEINS [J].
BURLEY, SK ;
PETSKO, GA .
FEBS LETTERS, 1986, 203 (02) :139-143
[7]   THE INTERNAL QUATERNARY AMMONIUM RECEPTOR-SITE OF SHAKER POTASSIUM CHANNELS [J].
CHOI, KL ;
MOSSMAN, C ;
AUBE, J ;
YELLEN, G .
NEURON, 1993, 10 (03) :533-541
[8]   EXPRESSION OF AN ATRIAL G-PROTEIN-ACTIVATED POTASSIUM CHANNEL IN XENOPUS-OOCYTES [J].
DASCAL, N ;
LIM, NF ;
SCHREIBMAYER, W ;
WANG, WZ ;
DAVIDSON, N ;
LESTER, HA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1993, 90 (14) :6596-6600
[9]   Coot:: model-building tools for molecular graphics [J].
Emsley, P ;
Cowtan, K .
ACTA CRYSTALLOGRAPHICA SECTION D-STRUCTURAL BIOLOGY, 2004, 60 :2126-2132
[10]   STRONG VOLTAGE-DEPENDENT INWARD RECTIFICATION OF INWARD RECTIFIER K+ CHANNELS IS CAUSED BY INTRACELLULAR SPERMINE [J].
FAKLER, B ;
BRANDLE, U ;
GLOWATZKI, E ;
WEIDEMANN, S ;
ZENNER, HP ;
RUPPERSBERG, JP .
CELL, 1995, 80 (01) :149-154