On the structural basis of modal gating behavior in K+ channels
Open Access
- 26 December 2010
- journal article
- research article
- Published by Springer Nature in Nature Structural & Molecular Biology
- Vol. 18 (1) , 67-74
- https://doi.org/10.1038/nsmb.1968
Abstract
The K+ channels can display three distinct gating modes. The molecular basis for two of these modes (low open probability and flickery) are now examined by a combination of single-channel recording, crystallography and modeling of mutants in Glu71, revealing that changes in ion and water occupancy in and around the selectivity filter determine modal gating. Modal-gating shifts represent an effective regulatory mechanism by which ion channels control the extent and time course of ionic fluxes. Under steady-state conditions, the K+ channel KcsA shows three distinct gating modes, high-Po, low-Po and a high-frequency flicker mode, each with about an order of magnitude difference in their mean open times. Here we show that in the absence of C-type inactivation, mutations at the pore-helix position Glu71 unmask a series of kinetically distinct modes of gating in a side chain–specific way. These gating modes mirror those seen in wild-type channels and suggest that specific interactions in the side chain network surrounding the selectivity filter, in concert with ion occupancy, alter the relative stability of pre-existing conformational states of the pore. The present results highlight the key role of the selectivity filter in regulating modal gating behavior in K+ channels.Keywords
This publication has 64 references indexed in Scilit:
- Structural mechanism of C-type inactivation in K+ channelsNature, 2010
- Atomic structure of a voltage-dependent K+ channel in a lipid membrane-like environmentNature, 2007
- A Quantitative Description of KcsA Gating II: Single-Channel CurrentsThe Journal of general physiology, 2007
- A Quantitative Description of KcsA Gating I: Macroscopic CurrentsThe Journal of general physiology, 2007
- Crystal structure of a Kir3.1-prokaryotic Kir channel chimeraThe EMBO Journal, 2007
- Detection of the Opening of the Bundle Crossing in KcsA with Fluorescence Lifetime Spectroscopy Reveals the Existence of Two Gates for Ion ConductionThe Journal of general physiology, 2006
- Scalable molecular dynamics with NAMDJournal of Computational Chemistry, 2005
- Crystal Structure of a Mammalian Voltage-Dependent Shaker Family K + ChannelScience, 2005
- Crystal structure and mechanism of a calcium-gated potassium channelNature, 2002
- CHARMM: A program for macromolecular energy, minimization, and dynamics calculationsJournal of Computational Chemistry, 1983