The KcsA potassium channel is a prototypical channel of bacterial origin, and the mechanism underlying the pH-dependent gating has been studied extensively. With the high-resolution atomic force microscopy (AFM), we have resolved functional open and closed gates of the KcsA channel under the membrane-embedded condition. Here we surprisingly found that the pH-dependent gating of the KcsA channels was associated with clustering–dispersion dynamics. At neutral pH, the resting, closed channels were coalesced, forming nanoclusters. At acidic pH, the open-gated channels were dispersed as singly isolated channels. Time-lapse AFM revealed reversible clustering–dispersion transitions upon pH changes. At acidic equilibrium, a small fraction of the ch...
AbstractActivation gating in KcsA is elicited by changes in intracellular proton concentration. Thom...
KirBac3.1 belongs to a family of transmembrane potassium (K(+)) channels that permit the selective f...
SummaryIon channels are signal transduction molecules that switch ion permeation pathways on and off...
The KcsA potassium channel is a prototypical channel of bacterial origin, and the mechanism underlyi...
Different patterns of channel activity have been detected by patch clamping excised membrane patches...
Mechanosensitive channels allow bacteria to respond to osmotic stress by opening a nanometer-sized p...
Mechanosensitive channels allow bacteria to respond to osmotic stress by opening a nanometer-sized p...
Ion conduction across the cellular membrane requires the simultaneous opening of activation and inac...
Crystallographic studies of channel proteins have provided insight into the molecular mechanisms of ...
AbstractMechanosensitive channels allow bacteria to respond to osmotic stress by opening a nanometer...
Full-text article is free to read on the publisher's website Mechanosensitive channels allow bacteri...
© 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. The segregation of cellular surfa...
The segregation of cellular surfaces in heterogeneous patches is considered to be a common motif in ...
The gating mechanism of a bacterial potassium channel, KcsA, has been investigated via multi-nanosec...
Artículo de publicación ISIThere is increasing evidence to support the notion that membrane protein...
AbstractActivation gating in KcsA is elicited by changes in intracellular proton concentration. Thom...
KirBac3.1 belongs to a family of transmembrane potassium (K(+)) channels that permit the selective f...
SummaryIon channels are signal transduction molecules that switch ion permeation pathways on and off...
The KcsA potassium channel is a prototypical channel of bacterial origin, and the mechanism underlyi...
Different patterns of channel activity have been detected by patch clamping excised membrane patches...
Mechanosensitive channels allow bacteria to respond to osmotic stress by opening a nanometer-sized p...
Mechanosensitive channels allow bacteria to respond to osmotic stress by opening a nanometer-sized p...
Ion conduction across the cellular membrane requires the simultaneous opening of activation and inac...
Crystallographic studies of channel proteins have provided insight into the molecular mechanisms of ...
AbstractMechanosensitive channels allow bacteria to respond to osmotic stress by opening a nanometer...
Full-text article is free to read on the publisher's website Mechanosensitive channels allow bacteri...
© 2017 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. The segregation of cellular surfa...
The segregation of cellular surfaces in heterogeneous patches is considered to be a common motif in ...
The gating mechanism of a bacterial potassium channel, KcsA, has been investigated via multi-nanosec...
Artículo de publicación ISIThere is increasing evidence to support the notion that membrane protein...
AbstractActivation gating in KcsA is elicited by changes in intracellular proton concentration. Thom...
KirBac3.1 belongs to a family of transmembrane potassium (K(+)) channels that permit the selective f...
SummaryIon channels are signal transduction molecules that switch ion permeation pathways on and off...