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Department of Physiology and Biophysics, University of Washington, Seattle, WA 98195

Address correspondence to Sharona E. Gordon, Department of Physiology and Biophysics, University of Washington, Seattle, WA 98195. Fax: (206) 685-5290; email: seg{at}u.washington.edu

Cyclic nucleotide–gated (CNG) ion channels are nonselective cation channels with a high permeability for Ca²⁺. Not surprisingly, they are blocked by a number of Ca²⁺ channel blockers including tetracaine, pimozide, and diltiazem. We studied the effects of dequalinium, an extracellular blocker of the small conductance Ca²⁺-activated K⁺ channel. We previously noted that dequalinium is a high-affinity blocker of CNGA1 channels from the intracellular side, with little or no state dependence at 0 mV. Here we examined block by dequalinium at a broad range of voltages in both CNGA1 and CNGA2 channels. We found that dequalinium block was mildly state dependent for both channels, with the affinity for closed channels 3–5 times higher than that for open channels. Mutations in the S4-S5 linker did not alter the affinity of open channels for dequalinium, but increased the affinity of closed channels by 10–20-fold. The state-specific effect of these mutations raises the question of whether/how the S4-S5 linker alters the binding of a blocker within the ion permeation pathway.

Key Words: CNG channels • dequalinium • voltage dependence • block • gating

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