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
[41]   Mechanism of rectification in inward-rectifier K+ channels [J].
Lu, Z .
ANNUAL REVIEW OF PHYSIOLOGY, 2004, 66 :103-129
[42]   ELECTROSTATIC TUNING OF MG2+ AFFINITY IN AN INWARD-RECTIFIER K+ CHANNEL [J].
LU, Z ;
MACKINNON, R .
NATURE, 1994, 371 (6494) :243-246
[43]   AMORE - AN AUTOMATED PACKAGE FOR MOLECULAR REPLACEMENT [J].
NAVAZA, J .
ACTA CRYSTALLOGRAPHICA SECTION A, 1994, 50 :157-163
[44]   Structural basis of inward rectification:: Cytoplasmic pore of the G protein-gated inward rectifier GIRK1 at 1.8 Å resolution [J].
Nishida, M ;
MacKinnon, R .
CELL, 2002, 111 (07) :957-965
[45]   Crystal structure of a Kir3.1-prokaryotic Kir channel chimera [J].
Nishida, Motohiko ;
Cadene, Martine ;
Chait, Brian T. ;
MacKinnon, Roderick .
EMBO JOURNAL, 2007, 26 (17) :4005-4015
[46]   ELECTRICAL PROPERTIES OF CARDIAC MUSCLE ATTRIBUTABLE TO INWARD GOING (ANOMALOUS) RECTIFICATION [J].
NOBLE, D .
JOURNAL OF CELLULAR AND COMPARATIVE PHYSIOLOGY, 1965, 66 (3P2S) :127-+
[47]   Processing of X-ray diffraction data collected in oscillation mode [J].
Otwinowski, Z ;
Minor, W .
MACROMOLECULAR CRYSTALLOGRAPHY, PT A, 1997, 276 :307-326
[48]   Cytoplasmic domain structures of Kir2.1 and Kir3.1 show sites for modulating gating and rectification [J].
Pegan, S ;
Arrabit, C ;
Zhou, W ;
Kwiatkowski, W ;
Collins, A ;
Slesinger, PA ;
Choe, S .
NATURE NEUROSCIENCE, 2005, 8 (03) :279-287
[49]   Evidence for sequential ion-binding Loci along the inner pore of the IRK1 inward-rectifier K+ channel [J].
Shin, HG ;
Xu, YP ;
Lu, Z .
JOURNAL OF GENERAL PHYSIOLOGY, 2005, 126 (02) :123-135
[50]   Mechanism of the voltage sensitivity of IRK1 inward-rectifier K+ channel block by the polyamine spermine [J].
Shin, HG ;
Lu, Z .
JOURNAL OF GENERAL PHYSIOLOGY, 2005, 125 (04) :413-426