In Shaker K+ channel, the amino terminus deletion Δ6-46 removes fast inactivation (N-type) unmasking a slow inactivation process. In Shaker Δ6-46 (Sh-IR) background, two additional mutations (T449V-I470C) remove slow inactivation, producing a noninactivating channel. However, despite the fact that Sh-IR-T449V-I470C mutant channels remain conductive, prolonged depolarizations (1 min, 0 mV) produce a shift of the QV curve by about −30 mV, suggesting that the channels still undergo the conformational changes typical of slow inactivation. For depolarizations longer than 50 ms, the tail currents measured during repolarization to −90 mV display a slow component that increases in amplitude as the duration of the depolarizing pulse increases. We found that the slow development of the QV shift had a counterpart in the amplitude of the slow component of the ionic tail current that is not present in Sh-IR. During long depolarizations, the time course of both the increase in the slow component of the tail current and the change in voltage dependence of the charge movement could be well fitted by exponential functions with identical time constant of 459 ms. Single channel recordings revealed that after prolonged depolarizations, the channels remain conductive for long periods after membrane repolarization. Nonstationary autocovariance analysis performed on macroscopic current in the T449V-I470C mutant confirmed that a novel open state appears with increasing prepulse depolarization time. These observations suggest that in the mutant studied, a new open state becomes progressively populated during long depolarizations (>50 ms). An appealing interpretation of these results is that the new open state of the mutant channel corresponds to a slow inactivated state of Sh-IR that became conductive.
Skip Nav Destination
Article navigation
1 February 2001
Article|
January 29 2001
A Conducting State with Properties of a Slow Inactivated State in a Shaker K+ Channel Mutant
Riccardo Olcese,
Riccardo Olcese
aDepartment of Anesthesiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
Search for other works by this author on:
Daniel Sigg,
Daniel Sigg
bDepartment of Physiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
Search for other works by this author on:
Ramon Latorre,
Ramon Latorre
dCentro de Estudios Científicos, Valdivia, Chile
eDepartamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile
Search for other works by this author on:
Francisco Bezanilla,
Francisco Bezanilla
aDepartment of Anesthesiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
bDepartment of Physiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
cDepartment of Brain Research Institute, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
Search for other works by this author on:
Enrico Stefani
Enrico Stefani
aDepartment of Anesthesiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
bDepartment of Physiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
cDepartment of Brain Research Institute, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
Search for other works by this author on:
Riccardo Olcese
aDepartment of Anesthesiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
Daniel Sigg
bDepartment of Physiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
Ramon Latorre
dCentro de Estudios Científicos, Valdivia, Chile
eDepartamento de Biología, Facultad de Ciencias, Universidad de Chile, Santiago, Chile
Francisco Bezanilla
aDepartment of Anesthesiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
bDepartment of Physiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
cDepartment of Brain Research Institute, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
Enrico Stefani
aDepartment of Anesthesiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
bDepartment of Physiology, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
cDepartment of Brain Research Institute, School of Medicine, University of California Los Angeles, Los Angeles, CA 90095
Abbreviations used in this paper: COP, conditional open probability; IC, inactivated conducting; INC, inactivated nonconducting.
Received:
August 07 2000
Revision Requested:
December 04 2000
Accepted:
January 02 2001
Online ISSN: 1540-7748
Print ISSN: 0022-1295
© 2001 The Rockefeller University Press
2001
The Rockefeller University Press
J Gen Physiol (2001) 117 (2): 149–164.
Article history
Received:
August 07 2000
Revision Requested:
December 04 2000
Accepted:
January 02 2001
Citation
Riccardo Olcese, Daniel Sigg, Ramon Latorre, Francisco Bezanilla, Enrico Stefani; A Conducting State with Properties of a Slow Inactivated State in a Shaker K+ Channel Mutant. J Gen Physiol 1 February 2001; 117 (2): 149–164. doi: https://doi.org/10.1085/jgp.117.2.149
Download citation file:
Sign in
Don't already have an account? Register
Client Account
You could not be signed in. Please check your email address / username and password and try again.
Could not validate captcha. Please try again.
Sign in via your Institution
Sign in via your InstitutionSuggested Content
Sodium Channel Inactivation Is Altered by Substitution of Voltage Sensor Positive Charges
J Gen Physiol (October,1997)
Allosteric Effects of Permeating Cations on Gating Currents during K+ Channel Deactivation
J Gen Physiol (August,1997)
Correlation between Charge Movement and Ionic Current during Slow Inactivation in Shaker K+ Channels
J Gen Physiol (November,1997)
Email alerts
Advertisement