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Biophys J
2007 Dec 15;9312:4209-24. doi: 10.1529/biophysj.107.104794.
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Speeding the recovery from ultraslow inactivation of voltage-gated Na+ channels by metal ion binding to the selectivity filter: a foot-on-the-door?
Szendroedi J, Sandtner W, Zarrabi T, Zebedin E, Hilber K, Dudley SC, Fozzard HA, Todt H.
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Slow inactivated states in voltage-gated ion channels can be modulated by binding molecules both to the outside and to the inside of the pore. Thus, external K(+) inhibits C-type inactivation in Shaker K(+) channels by a "foot-in-the-door" mechanism. Here, we explore the modulation of a very long-lived inactivated state, ultraslow inactivation (I(US)), by ligand binding to the outer vestibule in voltage-gated Na(+) channels. Blocking the outer vestibule by a mutant mu-conotoxin GIIIA substantially accelerated recovery from I(US). A similar effect was observed if Cd(2+) was bound to a cysteine engineered to the selectivity filter (K1237C). In K1237C channels, exposed to 30 microM Cd(2+), the time constant of recovery from I(US) was decreased from 145.0 +/- 10.2 s to 32.5 +/- 3.3 s (P < 0.001). Recovery from I(US) was only accelerated if Cd(2+) was added to the bath solution during recovery (V = -120 mV) from I(US), but not when the channels were selectively exposed to Cd(2+) during the development of I(US) (-20 mV). These data could be explained by a kinetic model in which Cd(2+) binds with high affinity to a slow inactivated state (I(S)), which is transiently occupied during recovery from I(US). A total of 50 microM Cd(2+) produced an approximately 8 mV hyperpolarizing shift of the steady-state inactivation curve of I(S), supporting this kinetic model. Binding of lidocaine to the internal vestibule significantly reduced the number of channels entering I(US), suggesting that I(US) is associated with a conformational change of the internal vestibule of the channel. We propose a molecular model in which slow inactivation (I(S)) occurs by a closure of the outer vestibule, whereas I(US) arises from a constriction of the internal vestibule produced by a widening of the selectivity filter region. Binding of Cd(2+) to C1237 promotes the closure of the selectivity filter region, thereby hastening recovery from I(US). Thus, Cd(2+) ions may act like a foot-on-the-door, kicking the I(S) gate to close.
Abdulla,
Changes in Na(+) channel currents of rat dorsal root ganglion neurons following axotomy and axotomy-induced autotomy.
2002, Pubmed
Abdulla,
Changes in Na(+) channel currents of rat dorsal root ganglion neurons following axotomy and axotomy-induced autotomy.
2002,
Pubmed Armstrong,
Interaction of tetraethylammonium ion derivatives with the potassium channels of giant axons.
1971,
Pubmed Balser,
External pore residue mediates slow inactivation in mu 1 rat skeletal muscle sodium channels.
1996,
Pubmed
,
Xenbase Balser,
Functional consequences of lidocaine binding to slow-inactivated sodium channels.
1996,
Pubmed
,
Xenbase Baukrowitz,
Modulation of K+ current by frequency and external [K+]: a tale of two inactivation mechanisms.
1995,
Pubmed Bean,
Lidocaine block of cardiac sodium channels.
1983,
Pubmed Becker,
Action of derivatives of mu-conotoxin GIIIA on sodium channels. Single amino acid substitutions in the toxin separately affect association and dissociation rates.
1992,
Pubmed Bénitah,
Molecular motions within the pore of voltage-dependent sodium channels.
1997,
Pubmed
,
Xenbase Black,
Sensory neuron-specific sodium channel SNS is abnormally expressed in the brains of mice with experimental allergic encephalomyelitis and humans with multiple sclerosis.
2000,
Pubmed Blunck,
Detection of the opening of the bundle crossing in KcsA with fluorescence lifetime spectroscopy reveals the existence of two gates for ion conduction.
2006,
Pubmed Boehm,
ATP stimulates sympathetic transmitter release via presynaptic P2X purinoceptors.
1999,
Pubmed Cannon,
Ion-channel defects and aberrant excitability in myotonia and periodic paralysis.
1996,
Pubmed Chahine,
Extrapore residues of the S5-S6 loop of domain 2 of the voltage-gated skeletal muscle sodium channel (rSkM1) contribute to the mu-conotoxin GIIIA binding site.
1998,
Pubmed
,
Xenbase Chang,
Predominant interactions between mu-conotoxin Arg-13 and the skeletal muscle Na+ channel localized by mutant cycle analysis.
1998,
Pubmed
,
Xenbase Chen,
Lidocaine induces a slow inactivated state in rat skeletal muscle sodium channels.
2000,
Pubmed
,
Xenbase Chiamvimonvat,
Control of ion flux and selectivity by negatively charged residues in the outer mouth of rat sodium channels.
1996,
Pubmed
,
Xenbase Choi,
Tetraethylammonium blockade distinguishes two inactivation mechanisms in voltage-activated K+ channels.
1991,
Pubmed Cordero-Morales,
Molecular determinants of gating at the potassium-channel selectivity filter.
2006,
Pubmed Decher,
Binding site of a novel Kv1.5 blocker: a "foot in the door" against atrial fibrillation.
2006,
Pubmed
,
Xenbase Dudley,
A mu-conotoxin-insensitive Na+ channel mutant: possible localization of a binding site at the outer vestibule.
1995,
Pubmed Dudley,
mu-conotoxin GIIIA interactions with the voltage-gated Na(+) channel predict a clockwise arrangement of the domains.
2000,
Pubmed Elinder,
Metal ion effects on ion channel gating.
2003,
Pubmed Eriksson,
Modeling the structure of agitoxin in complex with the Shaker K+ channel: a computational approach based on experimental distance restraints extracted from thermodynamic mutant cycles.
2002,
Pubmed Favre,
On the structural basis for ionic selectivity among Na+, K+, and Ca2+ in the voltage-gated sodium channel.
1996,
Pubmed
,
Xenbase Featherstone,
Interaction between fast and slow inactivation in Skm1 sodium channels.
1996,
Pubmed
,
Xenbase Fedida,
Modulation of slow inactivation in human cardiac Kv1.5 channels by extra- and intracellular permeant cations.
1999,
Pubmed French,
Interactions between a pore-blocking peptide and the voltage sensor of the sodium channel: an electrostatic approach to channel geometry.
1996,
Pubmed Grissmer,
TEA prevents inactivation while blocking open K+ channels in human T lymphocytes.
1989,
Pubmed Heinemann,
Calcium channel characteristics conferred on the sodium channel by single mutations.
1992,
Pubmed
,
Xenbase Hilber,
The selectivity filter of the voltage-gated sodium channel is involved in channel activation.
2001,
Pubmed
,
Xenbase Hilber,
Selectivity filter residues contribute unequally to pore stabilization in voltage-gated sodium channels.
2005,
Pubmed
,
Xenbase Hilber,
Interaction between fast and ultra-slow inactivation in the voltage-gated sodium channel. Does the inactivation gate stabilize the channel structure?
2002,
Pubmed
,
Xenbase Hille,
Local anesthetics: hydrophilic and hydrophobic pathways for the drug-receptor reaction.
1977,
Pubmed Hondeghem,
Time- and voltage-dependent interactions of antiarrhythmic drugs with cardiac sodium channels.
1977,
Pubmed Huang,
Electrostatic recognition and induced fit in the kappa-PVIIA toxin binding to Shaker potassium channel.
2005,
Pubmed Hui,
Electrostatic and steric contributions to block of the skeletal muscle sodium channel by mu-conotoxin.
2002,
Pubmed Jiang,
C-type inactivation involves a significant decrease in the intracellular aqueous pore volume of Kv1.4 K+ channels expressed in Xenopus oocytes.
2003,
Pubmed
,
Xenbase Kambouris,
Mechanistic link between lidocaine block and inactivation probed by outer pore mutations in the rat micro1 skeletal muscle sodium channel.
1998,
Pubmed
,
Xenbase Kellenberger,
Movement of the Na+ channel inactivation gate during inactivation.
1996,
Pubmed
,
Xenbase Lange,
Toxin-induced conformational changes in a potassium channel revealed by solid-state NMR.
2006,
Pubmed
,
Xenbase Levy,
A voltage-dependent role for K+ in recovery from C-type inactivation.
1996,
Pubmed Levy,
Recovery from C-type inactivation is modulated by extracellular potassium.
1996,
Pubmed Li,
Novel structural determinants of mu-conotoxin (GIIIB) block in rat skeletal muscle (mu1) Na+ channels.
2000,
Pubmed Li,
Molecular basis of isoform-specific micro-conotoxin block of cardiac, skeletal muscle, and brain Na+ channels.
2003,
Pubmed Li,
Pore residues critical for mu-CTX binding to rat skeletal muscle Na+ channels revealed by cysteine mutagenesis.
1997,
Pubmed
,
Xenbase Li,
Clockwise domain arrangement of the sodium channel revealed by (mu)-conotoxin (GIIIA) docking orientation.
2001,
Pubmed Liu,
Gated access to the pore of a voltage-dependent K+ channel.
1997,
Pubmed López-Barneo,
Effects of external cations and mutations in the pore region on C-type inactivation of Shaker potassium channels.
1993,
Pubmed
,
Xenbase Lossin,
Epilepsy-associated dysfunction in the voltage-gated neuronal sodium channel SCN1A.
2003,
Pubmed Loussouarn,
Structure and dynamics of the pore of inwardly rectifying K(ATP) channels.
2000,
Pubmed Mullins,
Extracellular sodium interacts with the HERG channel at an outer pore site.
2002,
Pubmed Ogielska,
Functional consequences of a decreased potassium affinity in a potassium channel pore. Ion interactions and C-type inactivation.
1999,
Pubmed
,
Xenbase Ong,
A structural rearrangement in the sodium channel pore linked to slow inactivation and use dependence.
2000,
Pubmed Pardo,
Extracellular K+ specifically modulates a rat brain K+ channel.
1992,
Pubmed
,
Xenbase Pérez-García,
Structure of the sodium channel pore revealed by serial cysteine mutagenesis.
1996,
Pubmed
,
Xenbase Rasmusson,
Inactivation of voltage-gated cardiac K+ channels.
1998,
Pubmed Ray,
A trapped intracellular cation modulates K+ channel recovery from slow inactivation.
2006,
Pubmed Rich,
Crucial role of sodium channel fast inactivation in muscle fibre inexcitability in a rat model of critical illness myopathy.
2003,
Pubmed Sandtner,
Lidocaine: a foot in the door of the inner vestibule prevents ultra-slow inactivation of a voltage-gated sodium channel.
2004,
Pubmed
,
Xenbase Sun,
On the structural basis for size-selective permeation of organic cations through the voltage-gated sodium channel. Effect of alanine mutations at the DEKA locus on selectivity, inhibition by Ca2+ and H+, and molecular sieving.
1997,
Pubmed Sunami,
Sodium channel selectivity filter regulates antiarrhythmic drug binding.
1997,
Pubmed
,
Xenbase Swartz,
Towards a structural view of gating in potassium channels.
2004,
Pubmed Takahashi,
Enhanced slow inactivation by V445M: a sodium channel mutation associated with myotonia.
1999,
Pubmed Takahashi,
Mexiletine block of disease-associated mutations in S6 segments of the human skeletal muscle Na(+) channel.
2001,
Pubmed Todt,
Ultra-slow inactivation in mu1 Na+ channels is produced by a structural rearrangement of the outer vestibule.
1999,
Pubmed
,
Xenbase Tomaselli,
A mutation in the pore of the sodium channel alters gating.
1995,
Pubmed
,
Xenbase Townsend,
Effect of alkali metal cations on slow inactivation of cardiac Na+ channels.
1997,
Pubmed
,
Xenbase Townsend,
Anomalous effect of permeant ion concentration on peak open probability of cardiac Na+ channels.
1997,
Pubmed
,
Xenbase Tsushima,
Altered ionic selectivity of the sodium channel revealed by cysteine mutations within the pore.
1997,
Pubmed
,
Xenbase Valiyaveetil,
Ion selectivity in a semisynthetic K+ channel locked in the conductive conformation.
2006,
Pubmed Veldkamp,
Two distinct congenital arrhythmias evoked by a multidysfunctional Na(+) channel.
2000,
Pubmed Vilin,
A single residue differentiates between human cardiac and skeletal muscle Na+ channel slow inactivation.
2001,
Pubmed
,
Xenbase Wang,
Enhanced Na(+) channel intermediate inactivation in Brugada syndrome.
2000,
Pubmed Woodhull,
Ionic blockage of sodium channels in nerve.
1973,
Pubmed Xiong,
A conserved ring of charge in mammalian Na+ channels: a molecular regulator of the outer pore conformation during slow inactivation.
2006,
Pubmed
,
Xenbase Xiong,
Molecular motions of the outer ring of charge of the sodium channel: do they couple to slow inactivation?
2003,
Pubmed
,
Xenbase Zebedin,
Fiber type conversion alters inactivation of voltage-dependent sodium currents in murine C2C12 skeletal muscle cells.
2004,
Pubmed Zhang,
A negatively charged residue in the outer mouth of rat sodium channel determines the gating kinetics of the channel.
2003,
Pubmed