Spontaneous activity shifts at constant experimental conditions represent a widespread regulatory mechanism in ion channels. The molecular origins of these modal gating shifts are poorly understood. In the K+ channel KcsA, a multitude of fast activity shifts that emulate the native modal gating behaviour can be triggered by point-mutations in the hydrogen bonding network that controls the selectivity filter. Using solid-state NMR and molecular dynamics simulations in a variety of KcsA mutants, here we show that modal gating shifts in K+ channels are associated with important changes in the channel dynamics that strongly perturb the selectivity filter equilibrium conformation. Furthermore, our study reveals a drastically different motional a...
The selectivity filter of K(+) channels contains four ion binding sites (S1-S4) and serves dual func...
The complicated patterns of the single-channel currents in potassium ion channel KcsA are governed b...
Potassium channels are opened by ligands and/or membrane potential. In voltage-gated K(+) channels a...
Spontaneous activity shifts at constant experimental conditions represent a widespread regulatory me...
Modal-gating shifts represent an effective regulatory mechanism by which ion channels control the ex...
AbstractPotassium channels switch between closed and open conformations and selectively conduct K+ i...
Most potassium channels have two main gate locations, hosting an inner gate at the cytosolic entranc...
Ion conduction across the cellular membrane requires the simultaneous opening of activation and inac...
SummaryThe selectivity filter of potassium channels is the structural element directly responsible f...
Potassium (K+) channels can regulate ionic conduction through their pore by a mechanism, involving t...
X-ray crystallography has provided tremendous insight into the different structural states of membra...
Potassium (K (+)) channels can regulate ionic conduction through their pore by a mechanism, involvin...
SummaryX-ray crystallography has provided tremendous insight into the different structural states of...
AbstractThe single-channel conductance varies significantly between different members of the inward ...
K2P potassium channels regulate cellular excitability using their selectivity filter (C-type) gate. ...
The selectivity filter of K(+) channels contains four ion binding sites (S1-S4) and serves dual func...
The complicated patterns of the single-channel currents in potassium ion channel KcsA are governed b...
Potassium channels are opened by ligands and/or membrane potential. In voltage-gated K(+) channels a...
Spontaneous activity shifts at constant experimental conditions represent a widespread regulatory me...
Modal-gating shifts represent an effective regulatory mechanism by which ion channels control the ex...
AbstractPotassium channels switch between closed and open conformations and selectively conduct K+ i...
Most potassium channels have two main gate locations, hosting an inner gate at the cytosolic entranc...
Ion conduction across the cellular membrane requires the simultaneous opening of activation and inac...
SummaryThe selectivity filter of potassium channels is the structural element directly responsible f...
Potassium (K+) channels can regulate ionic conduction through their pore by a mechanism, involving t...
X-ray crystallography has provided tremendous insight into the different structural states of membra...
Potassium (K (+)) channels can regulate ionic conduction through their pore by a mechanism, involvin...
SummaryX-ray crystallography has provided tremendous insight into the different structural states of...
AbstractThe single-channel conductance varies significantly between different members of the inward ...
K2P potassium channels regulate cellular excitability using their selectivity filter (C-type) gate. ...
The selectivity filter of K(+) channels contains four ion binding sites (S1-S4) and serves dual func...
The complicated patterns of the single-channel currents in potassium ion channel KcsA are governed b...
Potassium channels are opened by ligands and/or membrane potential. In voltage-gated K(+) channels a...