Fast inactivating Shaker H4 potassium channels and nonconducting pore mutant Shaker H4 W434F channels have been used to correlate the installation and recovery of the fast inactivation of ionic current with changes in the kinetics of gating current known as “charge immobilization” (Armstrong, C.M., and F. Bezanilla. 1977. J. Gen. Physiol. 70:567–590.). Shaker H4 W434F gating currents are very similar to those of the conducting clone recorded in potassium-free solutions. This mutant channel allows the recording of the total gating charge return, even when returning from potentials that would largely inactivate conducting channels. As the depolarizing potential increased, the OFF gating currents decay phase at −90 mV return potential changed from a single fast component to at least two components, the slower requiring ∼200 ms for a full charge return. The charge immobilization onset and the ionic current decay have an identical time course. The recoveries of gating current (Shaker H4 W434F) and ionic current (Shaker H4) in 2 mM external potassium have at least two components. Both recoveries are similar at −120 and −90 mV. In contrast, at higher potentials (−70 and −50 mV), the gating charge recovers significantly more slowly than the ionic current. A model with a single inactivated state cannot account for all our data, which strongly support the existence of “parallel” inactivated states. In this model, a fraction of the charge can be recovered upon repolarization while the channel pore is occupied by the NH2-terminus region.
Skip Nav Destination
Article navigation
1 May 1998
Article|
May 01 1998
Fast Inactivation in Shaker K+ Channels : Properties of Ionic and Gating Currents
Michel J. Roux,
Michel J. Roux
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Search for other works by this author on:
Riccardo Olcese,
Riccardo Olcese
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Search for other works by this author on:
Ligia Toro,
Ligia Toro
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Search for other works by this author on:
Francisco Bezanilla,
Francisco Bezanilla
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Search for other works by this author on:
Enrico Stefani
Enrico Stefani
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Search for other works by this author on:
Michel J. Roux
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Riccardo Olcese
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Ligia Toro
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Francisco Bezanilla
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Enrico Stefani
From the *Department of Anesthesiology, ‡Department of Molecular and Medical Pharmacology, and §Department of Physiology, University of California, Los Angeles, Los Angeles, California 90095-1778; and ‖Conicet, Buenos Aires, Argentina 1033
Address correspondence to Dr. Enrico Stefani, UCLA, Dept. of Anesthesiology, BH-612 CHS, Box 951778, Los Angeles, CA 90095-1778. Fax: 310-825-6649; E-mail: [email protected]
Dr. Roux's present address is Laboratoire de Neurobiologie, Ecole Normale Supérieure, 75005 Paris, France.
Received:
January 07 1998
Accepted:
March 05 1998
Online ISSN: 1540-7748
Print ISSN: 0022-1295
1998
J Gen Physiol (1998) 111 (5): 625–638.
Article history
Received:
January 07 1998
Accepted:
March 05 1998
Citation
Michel J. Roux, Riccardo Olcese, Ligia Toro, Francisco Bezanilla, Enrico Stefani; Fast Inactivation in Shaker K+ Channels : Properties of Ionic and Gating Currents . J Gen Physiol 1 May 1998; 111 (5): 625–638. doi: https://doi.org/10.1085/jgp.111.5.625
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
Normal and Mutant Rhodopsin Activation Measured with the Early Receptor Current in a Unicellular Expression System
J Gen Physiol (October,1999)
On the Mechanism by which 4-Aminopyridine Occludes Quinidine Block of the Cardiac K+ Channel, hKv1.5
J Gen Physiol (April,1998)
Extracellular Mg2+ Modulates Slow Gating Transitions and the Opening of Drosophila Ether-à-Go-Go Potassium Channels
J Gen Physiol (February,2000)
Email alerts
Advertisement