We studied the effects of permeant ions on the gating of the large conductance Ca(2+)-activated K+ channel from rat skeletal muscle. Rb+ blockade of inward K+ current caused an increase in the open probability as though Rb+ occupancy of the pore interferes with channel closing. In support of this hypothesis, we directly measured the occupancy of the pore by the impermeant ion Cs+ and found that it strongly correlates with its effect on gating. This is consistent with the "foot-in-the-door" model of gating, which states that channels cannot close with an ion in the pore. However, because Rb+ and Cs+ not only slow the closing rate (as predicted by the model), but also speed the opening rate, our results are more consistent with a modified ver...
Motivated by the results of Neyton and Miller (1988. J. Gen. Physiol. 92:549–586), suggesting that t...
Using Ba2 1 as a probe, we performed a detailed characterization of an external K 1 binding site l...
The gating mechanism of transmembrane ion channels is crucial for understanding how these proteins c...
The gating kinetics of a Ca2+-activated K+ channel from adult rat muscle plasma membrane are studied...
Voltage-dependent Ca++-activated K+ channels from rat skeletal muscle were reconstituted into planar...
Single Ca++-activated K+ channels from rat muscle plasma membranes are inhibited by Ba++. A single B...
High-conductance Ca(2+)-activated K+ channels from rat skeletal muscle were incorporated into planar...
The mechanism(s) by which channels control the flux of ions is still unknown. In single channel reco...
International audiencePermeant ions can have significant effects on ion channel conformational chang...
AbstractKv4 potassium channels undergo rapid inactivation but do not seem to exhibit the classical N...
Ion permeation and channel gating are classically considered independent processes, but site-specifi...
The cells that make up living organisms are enclosed by hydrophobic membranes that restrict movement...
We studied the blocking actions of external Ca2+, Mg2+, Ca2+, and other multivalent ions on single C...
Currents flowing through single stretch-inactivated ion channels were recorded from cell-attached pa...
Currents flowing through single dihydropyridine-sensitive Ca2+ channels were recorded from cell-atta...
Motivated by the results of Neyton and Miller (1988. J. Gen. Physiol. 92:549–586), suggesting that t...
Using Ba2 1 as a probe, we performed a detailed characterization of an external K 1 binding site l...
The gating mechanism of transmembrane ion channels is crucial for understanding how these proteins c...
The gating kinetics of a Ca2+-activated K+ channel from adult rat muscle plasma membrane are studied...
Voltage-dependent Ca++-activated K+ channels from rat skeletal muscle were reconstituted into planar...
Single Ca++-activated K+ channels from rat muscle plasma membranes are inhibited by Ba++. A single B...
High-conductance Ca(2+)-activated K+ channels from rat skeletal muscle were incorporated into planar...
The mechanism(s) by which channels control the flux of ions is still unknown. In single channel reco...
International audiencePermeant ions can have significant effects on ion channel conformational chang...
AbstractKv4 potassium channels undergo rapid inactivation but do not seem to exhibit the classical N...
Ion permeation and channel gating are classically considered independent processes, but site-specifi...
The cells that make up living organisms are enclosed by hydrophobic membranes that restrict movement...
We studied the blocking actions of external Ca2+, Mg2+, Ca2+, and other multivalent ions on single C...
Currents flowing through single stretch-inactivated ion channels were recorded from cell-attached pa...
Currents flowing through single dihydropyridine-sensitive Ca2+ channels were recorded from cell-atta...
Motivated by the results of Neyton and Miller (1988. J. Gen. Physiol. 92:549–586), suggesting that t...
Using Ba2 1 as a probe, we performed a detailed characterization of an external K 1 binding site l...
The gating mechanism of transmembrane ion channels is crucial for understanding how these proteins c...