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
[31]  
Shieh CC, 2000, PHARMACOL REV, V52, P557
[32]   Sodium permeability of a cloned small-conductance calcium-activated potassium channel [J].
Shin, N ;
Soh, H ;
Chang, S ;
Kim, DH ;
Park, CS .
BIOPHYSICAL JOURNAL, 2005, 89 (05) :3111-3119
[33]  
STANFIELD PR, 1994, J PHYSIOL-LONDON, V478, P1
[34]   Ion conduction through C-type inactivated Shaker channels [J].
Starkus, JG ;
Kuschel, L ;
Rayner, MD ;
Heinemann, SH .
JOURNAL OF GENERAL PHYSIOLOGY, 1997, 110 (05) :539-550
[35]   Inward rectification by polyamines in mouse Kir2.1 channels: synergy between blocking components [J].
Xie, LH ;
John, SA ;
Weiss, JN .
JOURNAL OF PHYSIOLOGY-LONDON, 2003, 550 (01) :67-82
[36]   CONTROL OF RECTIFICATION AND PERMEATION BY RESIDUES IN 2 DISTINCT DOMAINS IN AN INWARD RECTIFIER K+ CHANNEL [J].
YANG, J ;
JAN, YN ;
JAN, LY .
NEURON, 1995, 14 (05) :1047-1054
[37]   Stabilization of ion selectivity filter by pore loop ion pairs in an inwardly rectifying potassium channel [J].
Yang, J ;
Yu, M ;
Jan, YN ;
Jan, LY .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (04) :1568-1572
[38]   Yeast screen for constitutively active mutant G protein-activated potassium channels [J].
Yi, BA ;
Lin, YF ;
Jan, YN ;
Jan, LY .
NEURON, 2001, 29 (03) :657-667
[39]   Selectivity changes during activation of mutant Shaker potassium channels [J].
Zheng, J ;
Sigworth, FJ .
JOURNAL OF GENERAL PHYSIOLOGY, 1997, 110 (02) :101-117