Gating charge immobilization caused by the transition between inactivated states in the Kv1.5 channel

Citation
Zr. Wang et D. Fedida, Gating charge immobilization caused by the transition between inactivated states in the Kv1.5 channel, BIOPHYS J, 81(5), 2001, pp. 2614-2627
Citations number
25
Categorie Soggetti
Biochemistry & Biophysics
Journal title
BIOPHYSICAL JOURNAL
ISSN journal
00063495 → ACNP
Volume
81
Issue
5
Year of publication
2001
Pages
2614 - 2627
Database
ISI
SICI code
0006-3495(200111)81:5<2614:GCICBT>2.0.ZU;2-H
Abstract
Sustained Na+ or Li+ conductance is a feature of the inactivated state in w ild-type (WT) and nonconducting Shaker and Kv1.5 channels, and has been use d here to investigate the cause of off-gating charge immobilization in WT a nd Kv1.5-W472F nonconducting mutant channels. Off-gating immobilization in response to brief pulses in cells perfused with NMG(i)(+)/NMG(o)(+) is the result of a more negative voltage dependence of charge recovery (V-1/2 is - 96 mV) compared with on-gating charge movement (V-1/2 is -6.3 mV). This shi ft is known to be associated with slow inactivation in Shaker channels and the disparity is reduced by 40 mV, or similar to 50% in the presence of 135 mM Cs-i(+). Off-gating charge immobilization is voltage-dependent with a V -1/2 of - 12 mV, and correlates well with the development of Na+ conductanc e on repolarization through C-type inactivated channels (V-1/2 is -11 mV). As well, the time-dependent development of the inward Na+ tail current and gating charge immobilization after depolarizing pulses of different duratio ns has the same time constant (tau = 2.7 ms). These results indicate that i n Kv1.5 channels the transition to a stable C-type inactivated state takes only 2-3 ms and results in strong charge immobilization in the absence of G roup 1A metal cations, or even in the presence of Na-o(+). Inclusion of low concentrations of Cst delays the appearance of Na+ tail currents in WT cha nnels, prevents transition to inactivated states in Kv1.5-W472F nonconducti ng mutant channels, and removes charge immobilization. Higher concentration s of Cst are able to modulate the deactivating transition in Kv1.5 channels and prevent the residual slowing of charge return.