In this study, the authors investigated the mechanism of divalent cation block in a prokaryotic sodium channel, NavAb, by studying its mutants. They found that mutations increasing the hydrophilicity of the inner vestibule of the channel enabled a divalent cation to stack on the ion pathway. Molecular dynamics simulations showed that the stacking calcium ion repelled sodium ions at the bottom of the selectivity filter, providing insight into the primary process of divalent cation block in tetrameric cation channels.
Divalent cation block is observed in various tetrameric ion channels. For blocking, a divalent cation is thought to bind in the ion pathway of the channel, but such block has not yet been directly observed. So, the behaviour of these blocking divalent cations remains still uncertain. Here, we elucidated the mechanism of the divalent cation block by reproducing the blocking effect into NavAb, a well-studied tetrameric sodium channel. Our crystal structures of NavAb mutants show that the mutations increasing the hydrophilicity of the inner vestibule of the pore domain enable a divalent cation to stack on the ion pathway. Furthermore, non-equilibrium molecular dynamics simulation showed that the stacking calcium ion repel sodium ion at the bottom of the selectivity filter. These results suggest the primary process of the divalent cation block mechanism in tetrameric cation channels. Divalent cation block is observed in various tetrameric ion channels. Here, authors use X-ray crystallography, electrophysiology and molecular dynamics simulations to reveal the mechanism of the divalent cation block on a prokaryotic sodium channel.
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