Literature DB >> 11687881

Gating properties of inward-rectifier potassium channels: effects of permeant ions.

H Choe1, H Sackin, L G Palmer.   

Abstract

Two inward-rectifier K+ channels, ROMK2 (Kir1.1b) and IRK1 (Kir2.1), were expressed in Xenopus oocytes and their gating properties were studied in cell-attached membrane patches. The gating properties depended strongly on the ion being conducted (K+, NH4+, Rb+, or Tl+), suggesting tight coupling between permeation and gating. Mean open times were strongly dependent on the nature of the conducted ion. For ROMK2 the order from the longest to the shortest times was K+ > Rb+ > Tl+ > NH4+. For IRK1 the sequence was K+ > NH4+ > Tl+. In both cases the open times decreased monotonically as the membrane voltage was hyperpolarized. Both the absolute values and the voltage dependence of closed times were dependent on the conducted species. ROMK2 showed a single closed state whose mean lifetimes were biphasic functions of voltage. The maxima were at various voltages for different ions. IRK1 had at least two closed states whose lifetimes decreased monotonically with K+, increased monotonically with Tl+, and were relatively constant with NH4+ as the conducted ion. We explain the ion-dependence of gating by assuming that the ions bind to a site within the permeation pathway, resulting in a stable, ion-dependent, closed state of the channel. The patterns of voltage-dependence of closed-state lifetimes, which are specific for different ions, can be explained by variations in the rate at which the bound ions leave the pore toward the inside or the outside of the cell.

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Year:  2001        PMID: 11687881     DOI: 10.1007/s00232-001-0076-3

Source DB:  PubMed          Journal:  J Membr Biol        ISSN: 0022-2631            Impact factor:   1.843


  13 in total

1.  A conserved arginine near the filter of Kir1.1 controls Rb/K selectivity.

Authors:  Henry Sackin; Mikheil Nanazashvili; Hui Li; Lawrence G Palmer; D Eric Walters
Journal:  Channels (Austin)       Date:  2010 May-Jun       Impact factor: 2.581

2.  Relationship between pore occupancy and gating in BK potassium channels.

Authors:  Rebecca A Piskorowski; Richard W Aldrich
Journal:  J Gen Physiol       Date:  2006-05       Impact factor: 4.086

3.  The pore helix is involved in stabilizing the open state of inwardly rectifying K+ channels.

Authors:  Noga Alagem; Semen Yesylevskyy; Eitan Reuveny
Journal:  Biophys J       Date:  2003-07       Impact factor: 4.033

4.  K channel gating by an affinity-switching selectivity filter.

Authors:  Antonius M J VanDongen
Journal:  Proc Natl Acad Sci U S A       Date:  2004-02-19       Impact factor: 11.205

5.  Regulation of gating by negative charges in the cytoplasmic pore in the Kir2.1 channel.

Authors:  Lai-Hua Xie; Scott A John; Bernard Ribalet; James N Weiss
Journal:  J Physiol       Date:  2004-09-30       Impact factor: 5.182

6.  Single-channel basis for the slow activation of the repolarizing cardiac potassium current, I(Ks).

Authors:  Daniel Werry; Jodene Eldstrom; Zhuren Wang; David Fedida
Journal:  Proc Natl Acad Sci U S A       Date:  2013-02-19       Impact factor: 11.205

7.  Isoprenaline-stimulated differential adrenergic response of K+ channels in skeletal muscle under hypokalaemic conditions.

Authors:  R J Geukes Foppen; J Siegenbeek Van Heukelom
Journal:  Pflugers Arch       Date:  2003-03-15       Impact factor: 3.657

Review 8.  A comprehensive guide to the ROMK potassium channel: form and function in health and disease.

Authors:  Paul A Welling; Kevin Ho
Journal:  Am J Physiol Renal Physiol       Date:  2009-05-20

9.  On the structural basis of modal gating behavior in K(+) channels.

Authors:  Sudha Chakrapani; Julio F Cordero-Morales; Vishwanath Jogini; Albert C Pan; D Marien Cortes; Benoît Roux; Eduardo Perozo
Journal:  Nat Struct Mol Biol       Date:  2010-12-26       Impact factor: 15.369

Review 10.  Gating mechanism of KATP channels: function fits form.

Authors:  D Enkvetchakul; C G Nichols
Journal:  J Gen Physiol       Date:  2003-11       Impact factor: 4.086

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