Many calcium channels can distinguish between ions of the same charge but different size. For example, when cations are in direct competition with each other, the ryanodine receptor (RyR) calcium channel preferentially conducts smaller cations such as Li+ and Na+ over larger ones such as K+ and Cs+. Here, we analyze the physical basis for this preference using a previously established model of RyR permeation and selectivity. Like other calcium channels, RyR has four aspartate residues in its GGGIGDE selectivity filter. These aspartates have their terminal carboxyl group in the pore lumen, which take up much of the available space for permeating ions. We find that small ions are preferred by RyR because they can fit into this crowded environ...
AbstractIntracellular calcium release channels like ryanodine receptors (RyRs) and inositol trisphos...
AbstractL-type calcium channels are Ca2+ binding proteins of great biological importance. They gener...
Sequence comparison suggests that the ryanodine receptors (RyRs) have pore architecture similar to t...
Many calcium channels can distinguish between ions of the same charge but different size. For exampl...
AbstractMany calcium channels can distinguish between ions of the same charge but different size. Fo...
AbstractMany calcium channels can distinguish between ions of the same charge but different size. Fo...
AbstractA model of the ryanodine receptor (RyR) calcium channel is used to study the energetics of b...
AbstractA model of the ryanodine receptor (RyR) calcium channel is used to study the energetics of b...
Biological ion channels are proteins that passively conduct ions across membranes that are otherwise...
AbstractL-type calcium channels are Ca2+ binding proteins of great biological importance. They gener...
AbstractAnother research group has proposed an interesting model for calcium channel selectivity. Ho...
AbstractWe have tested the hypothesis that a high density of negative charge at the luminal mouth of...
AbstractCalcium channels have highly charged selectivity filters (4 COO− groups) that attract cation...
AbstractThe origin of the anomalous mole fraction effect (AMFE) in calcium channels is explored with...
AbstractSequence comparison suggests that the ryanodine receptors (RyRs) have pore architecture simi...
AbstractIntracellular calcium release channels like ryanodine receptors (RyRs) and inositol trisphos...
AbstractL-type calcium channels are Ca2+ binding proteins of great biological importance. They gener...
Sequence comparison suggests that the ryanodine receptors (RyRs) have pore architecture similar to t...
Many calcium channels can distinguish between ions of the same charge but different size. For exampl...
AbstractMany calcium channels can distinguish between ions of the same charge but different size. Fo...
AbstractMany calcium channels can distinguish between ions of the same charge but different size. Fo...
AbstractA model of the ryanodine receptor (RyR) calcium channel is used to study the energetics of b...
AbstractA model of the ryanodine receptor (RyR) calcium channel is used to study the energetics of b...
Biological ion channels are proteins that passively conduct ions across membranes that are otherwise...
AbstractL-type calcium channels are Ca2+ binding proteins of great biological importance. They gener...
AbstractAnother research group has proposed an interesting model for calcium channel selectivity. Ho...
AbstractWe have tested the hypothesis that a high density of negative charge at the luminal mouth of...
AbstractCalcium channels have highly charged selectivity filters (4 COO− groups) that attract cation...
AbstractThe origin of the anomalous mole fraction effect (AMFE) in calcium channels is explored with...
AbstractSequence comparison suggests that the ryanodine receptors (RyRs) have pore architecture simi...
AbstractIntracellular calcium release channels like ryanodine receptors (RyRs) and inositol trisphos...
AbstractL-type calcium channels are Ca2+ binding proteins of great biological importance. They gener...
Sequence comparison suggests that the ryanodine receptors (RyRs) have pore architecture similar to t...