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Biophys J
2015 Mar 24;1086:1435-1447. doi: 10.1016/j.bpj.2015.02.014.
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Sequence of gating charge movement and pore gating in HERG activation and deactivation pathways.
Goodchild SJ, Macdonald LC, Fedida D.
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KV11.1 voltage-gated K(+) channels are noted for unusually slow activation, fast inactivation, and slow deactivation kinetics, which tune channel activity to provide vital repolarizing current during later stages of the cardiac action potential. The bulk of charge movement in human ether-a-go-go-related gene (hERG) is slow, as is return of charge upon repolarization, suggesting that the rates of hERG channel opening and, critically, that of deactivation might be determined by slow voltage sensor movement, and also by a mode-shift after activation. To test these ideas, we compared the kinetics and voltage dependence of ionic activation and deactivation with gating charge movement. At 0 mV, gating charge moved ∼threefold faster than ionic current, which suggests the presence of additional slow transitions downstream of charge movement in the physiological activation pathway. A significant voltage sensor mode-shift was apparent by 24 ms at +60 mV in gating currents, and return of charge closely tracked pore closure after pulses of 100 and 300 ms duration. A deletion of the N-terminus PAS domain, mutation R4AR5A or the LQT2-causing mutation R56Q gave faster-deactivating channels that displayed an attenuated mode-shift of charge. This indicates that charge movement is perturbed by N- and C-terminus interactions, and that these domain interactions stabilize the open state and limit the rate of charge return. We conclude that slow on-gating charge movement can only partly account for slow hERG ionic activation, and that the rate of pore closure has a limiting role in the slow return of gating charges.
Arrigoni,
The voltage-sensing domain of a phosphatase gates the pore of a potassium channel.
2013, Pubmed,
Xenbase
Arrigoni,
The voltage-sensing domain of a phosphatase gates the pore of a potassium channel.
2013,
Pubmed
,
Xenbase Bezanilla,
The voltage sensor in voltage-dependent ion channels.
2000,
Pubmed Bezanilla,
Distribution and kinetics of membrane dielectric polarization. 1. Long-term inactivation of gating currents.
1982,
Pubmed Blunck,
Mechanism of electromechanical coupling in voltage-gated potassium channels.
2012,
Pubmed Chen,
Long QT syndrome-associated mutations in the Per-Arnt-Sim (PAS) domain of HERG potassium channels accelerate channel deactivation.
1999,
Pubmed
,
Xenbase Chen,
Allosteric effects of permeating cations on gating currents during K+ channel deactivation.
1997,
Pubmed Cheng,
Voltage-dependent gating of HERG potassium channels.
2012,
Pubmed Eldstrom,
The voltage-gated channel accessory protein KCNE2: multiple ion channel partners, multiple ways to long QT syndrome.
2011,
Pubmed Es-Salah-Lamoureux,
Fluorescence-tracking of activation gating in human ERG channels reveals rapid S4 movement and slow pore opening.
2010,
Pubmed
,
Xenbase Fedida,
Slow gating charge immobilization in the human potassium channel Kv1.5 and its prevention by 4-aminopyridine.
1996,
Pubmed Ferrer,
The S4-S5 linker directly couples voltage sensor movement to the activation gate in the human ether-a'-go-go-related gene (hERG) K+ channel.
2006,
Pubmed
,
Xenbase French,
Open-state stabilization in Kv channels: voltage-sensor relaxation and pore propping by a bound ion.
2012,
Pubmed Gianulis,
Direct interaction of eag domains and cyclic nucleotide-binding homology domains regulate deactivation gating in hERG channels.
2013,
Pubmed Goodchild,
Contributions of intracellular ions to kv channel voltage sensor dynamics.
2012,
Pubmed Goodchild,
Gating charge movement precedes ionic current activation in hERG channels.
2014,
Pubmed Goodchild,
Basis for allosteric open-state stabilization of voltage-gated potassium channels by intracellular cations.
2012,
Pubmed Gustina,
hERG potassium channel gating is mediated by N- and C-terminal region interactions.
2011,
Pubmed
,
Xenbase Gustina,
HERG potassium channel regulation by the N-terminal eag domain.
2012,
Pubmed Gustina,
A recombinant N-terminal domain fully restores deactivation gating in N-truncated and long QT syndrome mutant hERG potassium channels.
2009,
Pubmed
,
Xenbase Haddad,
Mode shift of the voltage sensors in Shaker K+ channels is caused by energetic coupling to the pore domain.
2011,
Pubmed
,
Xenbase Haitin,
The structural mechanism of KCNH-channel regulation by the eag domain.
2013,
Pubmed Hull,
Regional flexibility in the S4-S5 linker regulates hERG channel closed-state stabilization.
2014,
Pubmed
,
Xenbase January,
Long QT syndrome: cellular basis and arrhythmia mechanism in LQT2.
2000,
Pubmed Li,
Insight into the molecular interaction between the cyclic nucleotide-binding homology domain and the eag domain of the hERG channel.
2014,
Pubmed Melishchuk,
Mechanism underlying slow kinetics of the OFF gating current in Shaker potassium channel.
2001,
Pubmed Mitcheson,
A structural basis for drug-induced long QT syndrome.
2000,
Pubmed
,
Xenbase Morais Cabral,
Crystal structure and functional analysis of the HERG potassium channel N terminus: a eukaryotic PAS domain.
1998,
Pubmed
,
Xenbase Muskett,
Mechanistic insight into human ether-à-go-go-related gene (hERG) K+ channel deactivation gating from the solution structure of the EAG domain.
2011,
Pubmed Ng,
Multiple interactions between cytoplasmic domains regulate slow deactivation of Kv11.1 channels.
2014,
Pubmed
,
Xenbase Olcese,
Correlation between charge movement and ionic current during slow inactivation in Shaker K+ channels.
1997,
Pubmed
,
Xenbase Perozo,
Gating currents in Shaker K+ channels. Implications for activation and inactivation models.
1992,
Pubmed
,
Xenbase Piper,
Voltage sensor movement in the hERG K+ channel.
2005,
Pubmed Piper,
Gating currents associated with intramembrane charge displacement in HERG potassium channels.
2003,
Pubmed
,
Xenbase Priest,
S3-S4 linker length modulates the relaxed state of a voltage-gated potassium channel.
2013,
Pubmed Sanguinetti,
Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel.
1996,
Pubmed
,
Xenbase Sanguinetti,
A mechanistic link between an inherited and an acquired cardiac arrhythmia: HERG encodes the IKr potassium channel.
1995,
Pubmed
,
Xenbase Sanguinetti,
Delayed rectifier outward K+ current is composed of two currents in guinea pig atrial cells.
1991,
Pubmed Sanguinetti,
hERG potassium channels and cardiac arrhythmia.
2006,
Pubmed Schönherr,
Molecular determinants for activation and inactivation of HERG, a human inward rectifier potassium channel.
1996,
Pubmed
,
Xenbase Schönherr,
Functional role of the slow activation property of ERG K+ channels.
1999,
Pubmed
,
Xenbase Smith,
The inward rectification mechanism of the HERG cardiac potassium channel.
1996,
Pubmed Smith,
Fast and slow voltage sensor movements in HERG potassium channels.
2002,
Pubmed
,
Xenbase Tan,
Voltage-sensing domain mode shift is coupled to the activation gate by the N-terminal tail of hERG channels.
2012,
Pubmed
,
Xenbase Thomson,
Concerted all-or-none subunit interactions mediate slow deactivation of human ether-à-go-go-related gene K+ channels.
2014,
Pubmed
,
Xenbase Thouta,
Proline scan of the HERG channel S6 helix reveals the location of the intracellular pore gate.
2014,
Pubmed
,
Xenbase Trudeau,
HERG, a human inward rectifier in the voltage-gated potassium channel family.
1995,
Pubmed Van Slyke,
Mutations within the S4-S5 linker alter voltage sensor constraints in hERG K+ channels.
2010,
Pubmed
,
Xenbase Varga,
Cations affect the rate of gating charge recovery in wild-type and W434F Shaker channels through a variety of mechanisms.
2002,
Pubmed
,
Xenbase Villalba-Galea,
S4-based voltage sensors have three major conformations.
2008,
Pubmed Wang,
Components of gating charge movement and S4 voltage-sensor exposure during activation of hERG channels.
2013,
Pubmed Wang,
A quantitative analysis of the activation and inactivation kinetics of HERG expressed in Xenopus oocytes.
1997,
Pubmed
,
Xenbase Warmke,
A family of potassium channel genes related to eag in Drosophila and mammals.
1994,
Pubmed Wicks,
Sensitivity of HCN channel deactivation to cAMP is amplified by an S4 mutation combined with activation mode shift.
2009,
Pubmed
,
Xenbase Wymore,
Tissue and species distribution of mRNA for the IKr-like K+ channel, erg.
1997,
Pubmed
,
Xenbase Yang,
Allelic variants in long-QT disease genes in patients with drug-associated torsades de pointes.
2002,
Pubmed