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.

Highlights

  • From the Department of Pharmacology and Physiology, University of Rochester Medical Center, Rochester, New York 14642 abstract We measured unidirectional Kϩ in- and efflux through an inward rectifier K channel (IRK1) expressed in Xenopus oocytes

  • Some of the properties of ion channels that are consistent with multi-ion pore occupancy include: (a) an apparent concentration-dependent ion selectivity, (b) a voltage sensitivity of pore block by ions that depends on the concentration of the permeant ion or the blocking ion, (c) pore current that is a nonmonotonic function of the mole fraction of two types of ions, and (d) deviations from the Ussing (1949) flux ratio test for independent ion movement

  • We found that a simple four-barrier, three-site permeation model can account for the IRK1 flux ratio, as well as the single channel current– voltage and conductance data

Read more

Summary

Potassium Channels

Some of the properties of ion channels that are consistent with multi-ion pore occupancy include: (a) an apparent concentration-dependent ion selectivity, (b) a voltage sensitivity of pore block by ions that depends on the concentration of the permeant ion or the blocking ion (or both), (c) pore current (or conductance or permeability ratio) that is a nonmonotonic function of the mole fraction of two types of ions (the so-called “anomalous mole-fraction effect”), and (d) deviations from the Ussing (1949) flux ratio test for independent ion movement This latter test, as applied by Hodgkin and Keynes (1955), relies on a modified form of the Ussing flux ratio test for independent ion movement: Address correspondence to Ted Begenisich, Department of Pharmacology & Physiology, Box 711, University of Rochester Medical Center, Rochester, NY 14642. We found that a simple four-barrier, three-site permeation model can account for the IRK1 flux ratio, as well as the single channel current– voltage and conductance data

Oocyte Preparation
Single Channel Measurements
Permeation Models
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.