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 ∼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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1 October 1998
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October 01 1998
Nonindependent K+ Movement through the Pore in IRK1 Potassium Channels
Per Stampe,
Per Stampe
From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642
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Jorge Arreola,
Jorge Arreola
From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642
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Patricia Pérez-Cornejo,
Patricia Pérez-Cornejo
From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642
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Ted Begenisich
Ted Begenisich
From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642
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Per Stampe
From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642
Jorge Arreola
From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642
Patricia Pérez-Cornejo
From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642
Ted Begenisich
From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642
Address correspondence to Ted Begenisich, Department of Pharmacology & Physiology, Box 711, University of Rochester Medical Center, Rochester, NY 14642. Fax: 716-244-9283; E-mail: [email protected]
Received:
April 16 1998
Accepted:
August 03 1998
Online ISSN: 1540-7748
Print ISSN: 0022-1295
1998
J Gen Physiol (1998) 112 (4): 475–484.
Article history
Received:
April 16 1998
Accepted:
August 03 1998
Citation
Per Stampe, Jorge Arreola, Patricia Pérez-Cornejo, Ted Begenisich; Nonindependent K+ Movement through the Pore in IRK1 Potassium Channels . J Gen Physiol 1 October 1998; 112 (4): 475–484. doi: https://doi.org/10.1085/jgp.112.4.475
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