This study provides the first characterization of Shab slow inactivation, suggesting it involves rearrangement of an internal segment of the pore rather than narrowing of the extracellular entry.
Answers are grounded in this paper and cite their sources.
Does not yet alter clinical K+ channel modulation; hypothesis-generating for Shab inactivation mechanisms and requires mammalian validation.
Herein, we report the first characterization of Shab slow inactivation. Open Shab channels inactivate within seconds, with two voltage-independent time constants. Additionally, Shab presents significant closed-state inactivation. We found that with short depolarizing pulses, shorter than the slowest inactivation time constant, the resulting inactivation curve has a marked U-shape, but as pulse duration increases, approaching steady-state conditions, the U-shape vanishes, and the resulting inactivation curves converge to the classical Boltzmann h∞ curve. Regarding the mechanism of inactivation, we found that external K (+) and TEA facilitate both open- and closed-state inactivation, while the cavity blocker quinidine hinders inactivation. These results together with our previous observations regarding the K (+) -dependent stability of the K (+) conductance, suggest the novel hypothesis that inactivation of Shab channels, and possibly that of other Kv channels whose inactivation is facilitated by K (+) , does not involve a significant narrowing of the extracellular entry of the pore. Instead, we hypothesize that there is only a rearrangement of a more internal segment of the pore that affects the central cavity and halts K (+) conduction.
No takes yet. Share an insight, caveat, or question.
Carrillo et al. (2013) studied this question.
Synapse has enriched 10 related papers. Consider them for comparative context: