Calcium-dependent Gating of MthK, a Prokaryotic Potassium Channel
Open Access
- 30 May 2006
- journal article
- research article
- Published by Rockefeller University Press in The Journal of general physiology
- Vol. 127 (6) , 673-685
- https://doi.org/10.1085/jgp.200609534
Abstract
MthK is a calcium-gated, inwardly rectifying, prokaryotic potassium channel. Although little functional information is available for MthK, its high-resolution structure is used as a model for eukaryotic Ca2+-dependent potassium channels. Here we characterize in detail the main gating characteristics of MthK at the single-channel level with special focus on the mechanism of Ca2+ activation. MthK has two distinct gating modes: slow gating affected mainly by Ca2+ and fast gating affected by voltage. Millimolar Ca2+ increases MthK open probability over 100-fold by mainly increasing the frequency of channel opening while leaving the opening durations unchanged. The Ca2+ dose–response curve displays an unusually high Hill coefficient (n = ∼8), suggesting strong coupling between Ca2+ binding and channel opening. Depolarization affects both the fast gate by dramatically reducing the fast flickers, and to a lesser extent, the slow gate, by increasing MthK open probability. We were able to capture the mechanistic features of MthK with a modified MWC model.Keywords
This publication has 50 references indexed in Scilit:
- Structures of the MthK RCK Domain and the Effect of Ca2+ on Gating Ring StabilityJournal of Biological Chemistry, 2005
- X-ray structure of a voltage-dependent K+ channelNature, 2003
- Multiple regulatory sites in large-conductance calcium-activated potassium channelsNature, 2002
- The open pore conformation of potassium channelsNature, 2002
- Crystal structure and mechanism of a calcium-gated potassium channelNature, 2002
- Allosteric Regulation of Bk Channel Gating by Ca2+ and Mg2+ through a Nonselective, Low Affinity Divalent Cation SiteThe Journal of general physiology, 2001
- Single Streptomyces lividans K+ ChannelsThe Journal of general physiology, 1999
- A novel calcium-sensing domain in the BK channelBiophysical Journal, 1997
- The charybdotoxin family of K+ channel-blocking peptidesNeuron, 1995
- Design, synthesis, and functional expression of a gene for charybdotoxin, a peptide blocker of K+ channels.Proceedings of the National Academy of Sciences, 1991