Skip to Content
Merck
  • Basis for allosteric open-state stabilization of voltage-gated potassium channels by intracellular cations.

Basis for allosteric open-state stabilization of voltage-gated potassium channels by intracellular cations.

The Journal of general physiology (2012-10-17)
Samuel J Goodchild, Hongjian Xu, Zeineb Es-Salah-Lamoureux, Christopher A Ahern, David Fedida
ABSTRACT

The open state of voltage-gated potassium (Kv) channels is associated with an increased stability relative to the pre-open closed states and is reflected by a slowing of OFF gating currents after channel opening. The basis for this stabilization is usually assigned to intrinsic structural features of the open pore. We have studied the gating currents of Kv1.2 channels and found that the stabilization of the open state is instead conferred largely by the presence of cations occupying the inner cavity of the channel. Large impermeant intracellular cations such as N-methyl-d-glucamine (NMG(+)) and tetraethylammonium cause severe slowing of channel closure and gating currents, whereas the smaller cation, Cs(+), displays a more moderate effect on voltage sensor return. A nonconducting mutant also displays significant open state stabilization in the presence of intracellular K(+), suggesting that K(+) ions in the intracellular cavity also slow pore closure. A mutation in the S6 segment used previously to enlarge the inner cavity (Kv1.2-I402C) relieves the slowing of OFF gating currents in the presence of the large NMG(+) ion, suggesting that the interaction site for stabilizing ions resides within the inner cavity and creates an energetic barrier to pore closure. The physiological significance of ionic occupation of the inner cavity is underscored by the threefold slowing of ionic current deactivation in the wild-type channel compared with Kv1.2-I402C. The data suggest that internal ions, including physiological concentrations of K(+), allosterically regulate the deactivation kinetics of the Kv1.2 channel by impairing pore closure and limiting the return of voltage sensors. This may represent a primary mechanism by which Kv channel deactivation kinetics is linked to ion permeation and reveals a novel role for channel inner cavity residues to indirectly regulate voltage sensor dynamics.

MATERIALS
Product Number
Brand
Product Description

Sigma-Aldrich
Tetraethylammonium iodide, 98%
Sigma-Aldrich
Cesium, ingot, ≥99.95% trace metals basis
Sigma-Aldrich
Tetraethylammonium hydroxide solution, 20 wt. % in H2O
Supelco
Tetraethylammonium hydroxide solution, ~1.0 M (CH3CH2)4NOH in H2O, electrochemical grade
Sigma-Aldrich
Tetraethylammonium hydroxide solution, 35 wt. % in H2O
Sigma-Aldrich
Tetraethylammonium bromide, ReagentPlus®, 99%
Sigma-Aldrich
Tetraethylammonium bromide, reagent grade, 98%
Sigma-Aldrich
Tetraethylammonium chloride, BioUltra, for molecular biology, ≥99.0% (AT)
Supelco
Tetraethylammonium chloride, for electrochemical analysis, ≥99.0%
Sigma-Aldrich
Tetraethylammonium hydroxide solution, ~25% in methanol (~1.5 M)
Sigma-Aldrich
Tetraethylammonium chloride, ≥98% (titration)