Literature DB >> 9758865

Nonindependent K+ movement through the pore in IRK1 potassium channels.

P Stampe1, J Arreola, P Pérez-Cornejo, T Begenisich.   

Abstract

We measured unidirectional K+ in- and efflux through an inward rectifier K channel (IRK1) expressed in Xenopus oocytes. The ratio of these unidirectional fluxes differed significantly from expectations based on independent ion movement. In an extracellular solution with a K+ concentration of 25 mM, the data were described by a Ussing flux-ratio exponent, n', of approximately 2.2 and was constant over a voltage range from -50 to -25 mV. This result indicates that the pore of IRK1 channels may be simultaneously occupied by at least three ions. The IRK1 n' value of 2.2 is significantly smaller than the value of 3.5 obtained for Shaker K channels under identical conditions. To determine if other permeation properties that reflect multi-ion behavior differed between these two channel types, we measured the conductance (at 0 mV) of single IRK1 channels as a function of symmetrical K+ concentration. The conductance could be fit by a saturating hyperbola with a half-saturation K+ activity of 40 mM, substantially less than the reported value of 300 mM for Shaker K channels. We investigated the ability of simple permeation models based on absolute reaction rate theory to simulate IRK1 current-voltage, conductance, and flux-ratio data. Certain classes of four-barrier, three-site permeation models are inconsistent with the data, but models with high lateral barriers and a deep central well were able to account for the flux-ratio and single channel data. We conclude that while the pore in IRK1 and Shaker channels share important similarities, including K+ selectivity and multi-ion occupancy, they differ in other properties, including the sensitivity of pore conductance to K+ concentration, and may differ in the number of K+ ions that can simultaneously occupy the pore: IRK1 channels may contain three ions, but the pore in Shaker channels can accommodate four or more ions.

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Year:  1998        PMID: 9758865      PMCID: PMC2229430          DOI: 10.1085/jgp.112.4.475

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  35 in total

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Authors:  D A Doyle; J Morais Cabral; R A Pfuetzner; A Kuo; J M Gulbis; S L Cohen; B T Chait; R MacKinnon
Journal:  Science       Date:  1998-04-03       Impact factor: 47.728

2.  Inward rectification of the IRK1 K+ channel reconstituted in lipid bilayers.

Authors:  A Aleksandrov; B Velimirovic; D E Clapham
Journal:  Biophys J       Date:  1996-06       Impact factor: 4.033

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Authors:  R S Eisenberg
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4.  Permeation through an open channel: Poisson-Nernst-Planck theory of a synthetic ionic channel.

Authors:  D Chen; J Lear; B Eisenberg
Journal:  Biophys J       Date:  1997-01       Impact factor: 4.033

5.  Ion channel selectivity through stepwise changes in binding affinity.

Authors:  T X Dang; E W McCleskey
Journal:  J Gen Physiol       Date:  1998-02       Impact factor: 4.086

6.  Unidirectional K+ fluxes through recombinant Shaker potassium channels expressed in single Xenopus oocytes.

Authors:  P Stampe; T Begenisich
Journal:  J Gen Physiol       Date:  1996-04       Impact factor: 4.086

7.  [K+] dependence of open-channel conductance in cloned inward rectifier potassium channels (IRK1, Kir2.1).

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Journal:  Biophys J       Date:  1996-08       Impact factor: 4.033

8.  Spermine and spermidine as gating molecules for inward rectifier K+ channels.

Authors:  E Ficker; M Taglialatela; B A Wible; C M Henley; A M Brown
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9.  The interaction of Na+ and K+ in voltage-gated potassium channels. Evidence for cation binding sites of different affinity.

Authors:  L Kiss; D Immke; J LoTurco; S J Korn
Journal:  J Gen Physiol       Date:  1998-02       Impact factor: 4.086

10.  A conductance maximum observed in an inward-rectifier potassium channel.

Authors:  Z Lu; R MacKinnon
Journal:  J Gen Physiol       Date:  1994-09       Impact factor: 4.086

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  19 in total

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2.  Hierarchical approach to predicting permeation in ion channels.

Authors:  R J Mashl; Y Tang; J Schnitzer; E Jakobsson
Journal:  Biophys J       Date:  2001-11       Impact factor: 4.033

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4.  Ionic permeation and conduction properties of neuronal KCNQ2/KCNQ3 potassium channels.

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Journal:  Biophys J       Date:  2004-03       Impact factor: 4.033

5.  The bundle crossing region is responsible for the inwardly rectifying internal spermine block of the Kir2.1 channel.

Authors:  Chiung-Wei Huang; Chung-Chin Kuo
Journal:  Pflugers Arch       Date:  2013-07-20       Impact factor: 3.657

6.  Conduction of Na+ and K+ through the NaK channel: molecular and Brownian dynamics studies.

Authors:  Taira Vora; David Bisset; Shin-Ho Chung
Journal:  Biophys J       Date:  2008-05-02       Impact factor: 4.033

7.  Interaction between quaternary ammonium ions in the pore of potassium channels. Evidence against an electrostatic repulsion mechanism.

Authors:  J Thompson; T Begenisich
Journal:  J Gen Physiol       Date:  2000-06       Impact factor: 4.086

8.  Mechanism of the voltage sensitivity of IRK1 inward-rectifier K+ channel block by the polyamine spermine.

Authors:  Hyeon-Gyu Shin; Zhe Lu
Journal:  J Gen Physiol       Date:  2005-03-14       Impact factor: 4.086

9.  KcsA: it's a potassium channel.

Authors:  M LeMasurier; L Heginbotham; C Miller
Journal:  J Gen Physiol       Date:  2001-09       Impact factor: 4.086

10.  Mechanism of rectification in inward-rectifier K+ channels.

Authors:  Donglin Guo; Yajamana Ramu; Angela M Klem; Zhe Lu
Journal:  J Gen Physiol       Date:  2003-03-17       Impact factor: 4.086

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