Quaternary ammonium blockers inhibit many voltage-activated potassium (K⁺) channels from the intracellular side. When applied to Drosophila Shaker potassium channels expressed in mammalian cells, these rapidly reversible blockers produced use-dependent inhibition through an unusual mechanism-they promoted an intrinsic conformational change known as C-type inactivation, from which recovery is slow. The blockers did so by cutting off potassium ion flow to a site in the pore, which then emptied at a rate of 10⁵ ions per second. This slow rate probably reflected the departure of the last ion from the multi-ion pore: Permeation of ions (at 10⁷ per second) occurs rapidly because of ion-ion repulsion, but the last ion to leave would experience no such repulsion.