Potassium ion channels in the plasmalemma

1990 ◽  
Vol 79 (4) ◽  
pp. 705-711 ◽  
Author(s):  
Friedrich-Wilhelm Bentrup
2017 ◽  
Vol 129 (41) ◽  
pp. 12842-12845 ◽  
Author(s):  
Chao Lang ◽  
Xiaoli Deng ◽  
Feihu Yang ◽  
Bing Yang ◽  
Wei Wang ◽  
...  

1998 ◽  
Vol 26 (4) ◽  
pp. 188-199
Author(s):  
E Kyriacou

The study of molecular transport across gall-bladder epithelium may contribute to our understanding of the pathophysiology of gall-bladder disease. The aim of this study was to reconstitute and characterize single potassium ion channels in bovine gall-bladder epithelial mucosa – both apical and basolateral aspects. Standard subcellular fractionation techniques were used to form either apical or basolateral closed-membrane vesicles from the mucosal epithelium of fresh gall bladders from healthy young adult cattle. Vesicular ion channels were incorporated into voltage-clamped planar lipid bilayers under known ionic conditions and their conductances, reversal potentials, and voltages were characterized. Low-conductance voltage-insensitive apical membrane vesicle channels of at least four conductance levels were found (mean ± SD): 12 ± 4 pS, n = 10; 40 ± 12 pS, n = 4; 273 ± 31 pS, n = 3; and 151 ± 24 pS, n = 5. Conductances of potassium ion channels in basolateral membrane vesicles were in the range 9–450 pS, and these channels included high-conductance calcium-activated potassium-ion channels ‘K(Ca)’ which were voltage- and calcium-dependent.


Author(s):  
M. Kocmalova ◽  
M. Oravec ◽  
M. Adamkov ◽  
V. Sadlonova ◽  
I. Kazimierova ◽  
...  

2021 ◽  
pp. 507-545
Author(s):  
Janna Bednenko ◽  
Paul Colussi ◽  
Sunyia Hussain ◽  
Yihui Zhang ◽  
Theodore Clark

Author(s):  
Patricia S. Langan ◽  
Venu Gopal Vandavasi ◽  
Brendan Sullivan ◽  
Joel Harp ◽  
Kevin Weiss ◽  
...  

The mechanism by which potassium ions are transported through ion channels is currently being investigated by several groups using many different techniques. Clarification of the location of water molecules during transport is central to understanding how these integral membrane proteins function. Neutrons have a unique sensitivity to both hydrogen and potassium, rendering neutron crystallography capable of distinguishing waters from K+ ions. Here, the collection of a complete neutron data set from a potassium ion channel to a resolution of 3.55 Å using the Macromolecular Neutron Diffractometer (MaNDi) is reported. A room-temperature X-ray data set was also collected from the same crystal to a resolution of 2.50 Å. Upon further refinement, these results will help to further clarify the ion/water population within the selectivity filter of potassium ion channels.


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