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. 1996;35(7):867-75.
doi: 10.1016/0028-3908(96)00090-1.

Kinetic variability and modulation of dSlo, a cloned calcium-dependent potassium channel

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Kinetic variability and modulation of dSlo, a cloned calcium-dependent potassium channel

M R Bowlby et al. Neuropharmacology. 1996.

Abstract

We have examined, using patch recording, the modulation by ATP gamma S of the cloned Drosophila slopoke calcium-dependent potassium channel (dSlo) expressed in Xenopus oocytes. There is a large variation in the gating kinetics, open probability, and conductance level of the channel in this expression system, which complicates the analysis of modulatory events. Addition of ATP gamma S to the intracellular face of the patch does not consistently alter the overall open probability of dSlo, but it does increase the frequency of appearance of an exceptionally long-lived closed state of the channel. This modulation is not blocked by an inhibitor of several serine/threonine protein kinases, nor by mutation of a serine residue that is a target for phosphorylation by protein kinase A. Thus, ATP gamma S may alter dSlo kinetic properties by some mechanism other than serine/threonine phosphorylation.

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