Key result
Single-channel electrophysiology and x-ray crystallography revealed that Ba2+ blocks the MthK K+ channel at the internal side, with binding sites dependent on the presence of Na+ or K+.
This study identifies the molecular basis for Ba2+ blockade of K+ channels by demonstrating distinct binding site preferences depending on the ionic environment.
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Animal data on K+ channel block require cautious interpretation; leaves open relevance to mammalian physiology.
The movement and interaction of multiple ions passing through in single file underlie various fundamental K(+) channel properties, from the effective conduction of K(+) ions to channel blockade by Ba(2+) ions. In this study, we used single-channel electrophysiology and x-ray crystallography to probe the interactions of Ba(2+) with permeant ions within the ion conduction pathway of the MthK K(+) channel. We found that, as typical of K(+) channels, the MthK channel was blocked by Ba(2+) at the internal side, and the Ba(2+)-blocking effect was enhanced by external K(+). We also obtained crystal structures of the MthK K(+) channel pore in both Ba(2+)-Na(+) and Ba(2+)-K(+) environments. In the Ba(2+)-Na(+) environment, we found that a single Ba(2+) ion remained bound in the selectivity filter, preferably at site 2, whereas in the Ba(2+)-K(+) environment, Ba(2+) ions were predominantly distributed between sites 3 and 4. These ionic configurations are remarkably consistent with the functional studies and identify a molecular basis for Ba(2+) blockade of K(+) channels.
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Guo et al. (2014) studied this question. Ba2+ was evaluated on Ba2+ interaction with permeant ions within the ion conduction pathway of the MthK K+ channel. Single-channel electrophysiology and x-ray crystallography revealed that Ba2+ blocks the MthK K+ channel at the internal side, with binding sites dependent on the presence of Na+ or K+.
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