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PMID: 15138750 Published · ppublish English Journal Article Research Support, Non-U.S. Gov't

Rate-limiting reactions determining different activation kinetics of Kv1.2 and Kv2.1 channels.

The Journal of membrane biology ·Vol. 198 ·No. 2 ·2004-03-15 ·Pages 103-12

Scholle A, Dugarmaa S, Zimmer T, Leonhardt M, Koopmann R, Engeland B, Pongs O, Benndorf K

Abstract

To identify the mechanisms underlying the faster activation kinetics in Kv1.2 channels compared to Kv2.1 channels, ionic and gating currents were studied in rat Kv1.2 and human Kv2.1 channels heterologously expressed in mammalian cells. At all voltages the time course of the ionic currents could be described by an initial sigmoidal and a subsequent exponential component and both components were faster in Kv1.2 than in Kv2.1 channels. In Kv1.2 channels, the activation time course was more sigmoid at more depolarized potentials, whereas in Kv2.1 channels it was somewhat less sigmoid at more depolarized potentials. In contrast to the ionic currents, the ON gating currents were similarly fast for both channels. The main portion of the measured ON gating charge moved before the ionic currents were activated. The equivalent gating charge of Kv1.2 ionic currents was twice that of Kv2.1 ionic currents, whereas that of Kv1.2 ON gating currents was smaller than that of Kv2.1 ON gating currents. In conclusion, the different activation kinetics of Kv1.2 and Kv2.1 channels are caused by rate-limiting reactions that follow the charge movement recorded from the gating currents. In Kv1.2 channels, the reaction coupling the voltage-sensor movement to the pore opening contributes to rate limitation in a voltage-dependent fashion, whereas in Kv2.1 channels, activation is additionally rate-limited by a slow reaction in the subunit gating.

MeSH Terms
Animals CHO Cells Cricetinae Delayed Rectifier Potassium Channels Electrophysiology Humans Ion Channel Gating Kinetics Kv1.2 Potassium Channel Membrane Potentials Patch-Clamp Techniques Potassium Channels/metabolism Potassium Channels, Voltage-Gated Shab Potassium Channels
Chemicals
Delayed Rectifier Potassium Channels KCNA2 protein, human KCNB1 protein, human Kv1.2 Potassium Channel Potassium Channels Potassium Channels, Voltage-Gated Shab Potassium Channels
Authors & Affiliations
8 authors, click to expand affiliations / ORCID
Scholle A
Institut für Physiologie, Herz-Kreislauf-Physiologie, Friedrich-Schiller-Universität, 07740, Jena, Germany.
Dugarmaa S
Zimmer T
Leonhardt M
Koopmann R
Engeland B
Pongs O
Benndorf K
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Article Info
Journal
The Journal of membrane biology
Abbr.
J Membr Biol
ISSN
0022-2631
Published
2004-03-15
Pages
103-12
Language
English
Region
United States
NLM ID
0211301
Subset
IM
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