AbstractK+ channels can be occupied by multiple permeant ions that appear to bind at discrete locations in the conduction pathway. Neither the molecular nature of the binding sites nor their relation to the activation or inactivation gates that control ion flow are well understood. We used the permeant ion Ba2+ as a K+ analog to probe for K+ ion binding sites and their relationship to the activation and inactivation gates. Our data are consistent with the existence of three single-file permeant-ion binding sites: one deep site, which binds Ba2+ with high affinity, and two more external sites whose occupancy influences Ba2+ movement to and from the deep site. All three sites are accessible to the external solution in channels with a closed a...
AbstractHigh-affinity, intrapore binding of Ca2+ over competing ions is the essential feature in the...
AbstractMutations in the outer pore region of Shaker K+ channels (T449 and D447) can influence exter...
Selective ion channels play a crucial role in every aspect of life. The function has been intensivel...
AbstractK+ channels can be occupied by multiple permeant ions that appear to bind at discrete locati...
AbstractShaker K+ channels inactivate through two distinct molecular mechanisms: N-type, which invol...
Potassium channels are presumed to have two allosterically coupled gates, the activation gate and th...
AbstractWith prolonged or repetitive activation, voltage-gated K+ channels undergo a slow (C-type) i...
Voltage-dependent ion channels are presently thought to consist of several distinct functional regio...
Using Ba2 1 as a probe, we performed a detailed characterization of an external K 1 binding site l...
AbstractBased on the structure of the KcsA potassium channel, the Shaker K+ channel is thought to ha...
AbstractK+ are selectively coordinated in the selectivity filter and concerted K+ and water movement...
The gating mechanism of transmembrane ion channels is crucial for understanding how these proteins c...
The gating mechanism of transmembrane ion channels is crucial for understanding how these proteins c...
Motivated by the results of Neyton and Miller (1988. J. Gen. Physiol. 92:549–586), suggesting that t...
We have investigated some of the permeation properties of the pore in Shaker K channels. We determin...
AbstractHigh-affinity, intrapore binding of Ca2+ over competing ions is the essential feature in the...
AbstractMutations in the outer pore region of Shaker K+ channels (T449 and D447) can influence exter...
Selective ion channels play a crucial role in every aspect of life. The function has been intensivel...
AbstractK+ channels can be occupied by multiple permeant ions that appear to bind at discrete locati...
AbstractShaker K+ channels inactivate through two distinct molecular mechanisms: N-type, which invol...
Potassium channels are presumed to have two allosterically coupled gates, the activation gate and th...
AbstractWith prolonged or repetitive activation, voltage-gated K+ channels undergo a slow (C-type) i...
Voltage-dependent ion channels are presently thought to consist of several distinct functional regio...
Using Ba2 1 as a probe, we performed a detailed characterization of an external K 1 binding site l...
AbstractBased on the structure of the KcsA potassium channel, the Shaker K+ channel is thought to ha...
AbstractK+ are selectively coordinated in the selectivity filter and concerted K+ and water movement...
The gating mechanism of transmembrane ion channels is crucial for understanding how these proteins c...
The gating mechanism of transmembrane ion channels is crucial for understanding how these proteins c...
Motivated by the results of Neyton and Miller (1988. J. Gen. Physiol. 92:549–586), suggesting that t...
We have investigated some of the permeation properties of the pore in Shaker K channels. We determin...
AbstractHigh-affinity, intrapore binding of Ca2+ over competing ions is the essential feature in the...
AbstractMutations in the outer pore region of Shaker K+ channels (T449 and D447) can influence exter...
Selective ion channels play a crucial role in every aspect of life. The function has been intensivel...