Javascript must be enabled to continue!
Effects of Ionic Strength on Gating and Permeation of TREK-2 K2P channels
View through CrossRef
Abstract
In addition to the classical voltage-dependent behavior mediated by voltage-sensing-domains (VSD), a growing number of voltage-dependent gating behaviors are being described in ion channels that lack canonical VSDs. A common thread in their mechanism of action is the contribution of the permeating ion to this voltage sensing process. The polymodal K2P K
+
channel TREK2 responds to membrane voltage through a gating process that is mediated by the interaction of K
+
with its selectivity filter. Recently, we have found that this action can be modulated by small molecule agonists (e.g. BL1249) which appear to have an electrostatic influence on K
+
binding within the inner cavity and produce an increase in the single-channel conductance of TREK-2 channels. Here, we directly probed this K
+
-dependent gating process by recording both macroscopic and single-channel currents of TREK-2 in the presence of high concentrations of internal K
+
. Surprisingly we found that the channel is inhibited by high internal K
+
concentrations and that this is mediated by the concomitant increase in ionic-strength. However, we were still able to determine that the increase in single channel conductance in the presence of BL1249 was blunted in high ionic-strength, whilst its activatory effect (on channel open probability) persisted. These effects are consistent with an electrostatic mechanism of action of negatively charged activators such as BL1249 on permeation, but also suggest that their influence on channel gating is more complex.
Title: Effects of Ionic Strength on Gating and Permeation of TREK-2 K2P channels
Description:
Abstract
In addition to the classical voltage-dependent behavior mediated by voltage-sensing-domains (VSD), a growing number of voltage-dependent gating behaviors are being described in ion channels that lack canonical VSDs.
A common thread in their mechanism of action is the contribution of the permeating ion to this voltage sensing process.
The polymodal K2P K
+
channel TREK2 responds to membrane voltage through a gating process that is mediated by the interaction of K
+
with its selectivity filter.
Recently, we have found that this action can be modulated by small molecule agonists (e.
g.
BL1249) which appear to have an electrostatic influence on K
+
binding within the inner cavity and produce an increase in the single-channel conductance of TREK-2 channels.
Here, we directly probed this K
+
-dependent gating process by recording both macroscopic and single-channel currents of TREK-2 in the presence of high concentrations of internal K
+
.
Surprisingly we found that the channel is inhibited by high internal K
+
concentrations and that this is mediated by the concomitant increase in ionic-strength.
However, we were still able to determine that the increase in single channel conductance in the presence of BL1249 was blunted in high ionic-strength, whilst its activatory effect (on channel open probability) persisted.
These effects are consistent with an electrostatic mechanism of action of negatively charged activators such as BL1249 on permeation, but also suggest that their influence on channel gating is more complex.
Related Results
Tandem Pore Domain Potassium Channels
Tandem Pore Domain Potassium Channels
Abstract
The KCNK gene family encodes two-pore-domain potassium (K2P) channels, which generate the background (“leak”) K+ currents that establish a negative resting ...
Difference in current densities of two pore domain potassium channel between ventricular and ventricular outflow tract cardiomyocytes in rabbit heart
Difference in current densities of two pore domain potassium channel between ventricular and ventricular outflow tract cardiomyocytes in rabbit heart
Objective
Idiopathic ventricular tachycardia mainly originates from right ventricular outflow tract. It has been proved that cardiomyocytes in rabbit right ventri...
Molecular Dynamics Trajectory Analysis of Permeation (MDTAP): A tool to analyze permeation events across membrane proteins
Molecular Dynamics Trajectory Analysis of Permeation (MDTAP): A tool to analyze permeation events across membrane proteins
Abstract
Background and Objective
Molecular dynamics (MD) simulations are indispensable and versatile in capturing the time-dep...
Activation of hTREK-1 by polyunsaturated fatty acids does not only involve membrane tension
Activation of hTREK-1 by polyunsaturated fatty acids does not only involve membrane tension
ABSTRACT
TREK-1 is a mechanosensitive channel also activated by polyunsaturated fatty acids (PUFAs). In this study, we compared the effect of mul...
Activation of hTREK-1 by polyunsaturated fatty acids does not only involve membrane tension
Activation of hTREK-1 by polyunsaturated fatty acids does not only involve membrane tension
Abstract
TREK-1 is a mechanosensitive channel activated by polyunsaturated fatty acids (PUFAs). Its activation is supposed to be linked to changes in membrane tension follo...
Co-permeation of hydrogen isotopes in tungsten at high temperatures
Co-permeation of hydrogen isotopes in tungsten at high temperatures
The permeation behavior of hydrogen (H2)–deuterium (D2) mixtures with varying molar ratios through tungsten (W) was systematically investigated using the gas-driven permeation meth...
Activation of hTREK-1 by polyunsaturated fatty acids involves direct interaction
Activation of hTREK-1 by polyunsaturated fatty acids involves direct interaction
AbstractTREK-1 is a mechanosensitive channel activated by polyunsaturated fatty acids (PUFAs). Its activation is supposed to be linked to changes in membrane tension following PUFA...
Extraction of aromatic solvents from reformates and paint solvent wastes during ionic liquids
Extraction of aromatic solvents from reformates and paint solvent wastes during ionic liquids
The work conducted in this study comprised three aspects: syntheses, characterizations, and multi-component liquid-liquid extractions. The main objectives of the project were: (1) ...

