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 50 条
  • [41] A strongly inwardly rectifying K+ channel that is sensitive to ATP
    Collins, A
    German, MS
    Jan, YN
    Jan, LY
    Zhao, B
    JOURNAL OF NEUROSCIENCE, 1996, 16 (01) : 1 - 9
  • [42] Mechanism of activation at the selectivity filter of the KcsA K+ channel
    Heer, Florian T.
    Posson, David J.
    Wojtas-Niziurski, Wojciech
    Nimigean, Crina M.
    Berneche, Simon
    ELIFE, 2017, 6
  • [43] Initial steps of inactivation at the K+ channel selectivity filter
    Thomson, Andrew S.
    Heer, Florian T.
    Smith, Frank J.
    Hendron, Eunan
    Berneche, Simon
    Rothberg, Brad S.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2014, 111 (17) : E1713 - E1722
  • [44] Transfer of voltage independence from a rat olfactory channel to the Drosophila ether-a-go-go K+ channel
    Tang, CY
    Papazian, DM
    JOURNAL OF GENERAL PHYSIOLOGY, 1997, 109 (03) : 301 - 311
  • [45] TRESK background K+ channel deletion selectively uncovers enhanced mechanical and cold sensitivity
    Castellanos, Aida
    Pujol-Coma, Anna
    Andres-Bilbe, Alba
    Negm, Ahmed
    Callejo, Gerard
    Soto, David
    Noel, Jacques
    Comes, Nuria
    Gasull, Xavier
    JOURNAL OF PHYSIOLOGY-LONDON, 2020, 598 (05): : 1017 - 1038
  • [46] Digitalized K+ Occupancy in the Nanocavity Holds and Releases Queues of K+ in a Channel
    Sumikama, Takashi
    Oiki, Shigetoshi
    JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 2016, 138 (32) : 10284 - 10292
  • [47] Site-specific ion occupation in the selectivity filter causes voltage-dependent gating in a viral K+ channel
    Rauh, O.
    Hansen, U. P.
    Scheub, D. D.
    Thiel, G.
    Schroeder, I
    SCIENTIFIC REPORTS, 2018, 8
  • [48] The antipsychotic drugs sertindole and pimozide block erg3, a human brain K+ channel
    Kang, JS
    Chen, XL
    Rampe, D
    BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2001, 286 (03) : 499 - 504
  • [49] Effect of K+ and Rb+ on the action of verapamil on a voltage-gated K+ channel, hKv1.3: implications for a second open state?
    Kuras, Z.
    Grissmer, S.
    BRITISH JOURNAL OF PHARMACOLOGY, 2009, 157 (05) : 757 - 768
  • [50] Structural implications of hERG K+ channel block by a high-affinity minimally structured blocker
    Helliwell, Matthew V.
    Zhang, Yihong
    El Harchi, Aziza
    Du, Chunyun
    Hancox, Jules C.
    Dempsey, Christopher E.
    JOURNAL OF BIOLOGICAL CHEMISTRY, 2018, 293 (18) : 7040 - 7057