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2.
Biophys J ; 81(2): 814-26, 2001 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-11463627

RESUMEN

We previously concluded that the Kv2.1 K(+) channel inactivates preferentially from partially activated closed states. We report here that the Kv3.1 channel also exhibits two key features of this inactivation mechanism: a U-shaped voltage dependence measured at 10 s and stronger inactivation with repetitive pulses than with a single long depolarization. More surprisingly, slow inactivation of the Kv1 Shaker K(+) channel (Shaker B Delta 6--46) also has a U-shaped voltage dependence for 10-s depolarizations. The time and voltage dependence of recovery from inactivation reveals two distinct components for Shaker. Strong depolarizations favor inactivation that is reduced by K(o)(+) or by partial block by TEA(o), as previously reported for slow inactivation of Shaker. However, depolarizations near 0 mV favor inactivation that recovers rapidly, with strong voltage dependence (as for Kv2.1 and 3.1). The fraction of channels that recover rapidly is increased in TEA(o) or high K(o)(+). We introduce the term U-type inactivation for the mechanism that is dominant in Kv2.1 and Kv3.1. U-type inactivation also makes a major but previously unrecognized contribution to slow inactivation of Shaker.


Asunto(s)
Neuropéptidos/antagonistas & inhibidores , Neuropéptidos/metabolismo , Bloqueadores de los Canales de Potasio , Canales de Potasio con Entrada de Voltaje , Canales de Potasio/metabolismo , Regulación Alostérica/efectos de los fármacos , Animales , Proteínas de Drosophila , Drosophila melanogaster , Electrofisiología , Cinética , Potenciales de la Membrana/efectos de los fármacos , Modelos Biológicos , Neuropéptidos/genética , Oocitos/efectos de los fármacos , Oocitos/metabolismo , Canales de Potasio/genética , ARN/genética , ARN/metabolismo , Canales de Potasio de la Superfamilia Shaker , Canales de Potasio Shaw , Tetraetilamonio/farmacología , Xenopus laevis
3.
Am J Physiol Heart Circ Physiol ; 280(1): H354-60, 2001 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11123251

RESUMEN

Idiopathic ventricular fibrillation (IVF) can cause sudden death in both adults and children. One form of IVF (Brugada syndrome), characterized by S-T segment elevation (STE) in the electrocardiogram, has been linked to mutations of SCN5A, the gene encoding the voltage-gated cardiac Na(+) channel. A missense mutation of SCN5A that substitutes glutamine for leucine at codon 567 (L567Q, in the cytoplasmic linker between domains I and II) is identified with sudden infant death and Brugada syndrome in one family. However, neither the functional effect of the L567Q mutation nor the molecular mechanism underlying the pathogenicity of the mutation is known. Patch-clamp analysis of L567Q channels expressed in human embryonic kidney cells revealed a marked acceleration and a negative shift in the voltage dependence of inactivation. Unlike other Brugada mutations, this phenotype was expressed independently of temperature or auxiliary beta(1)-subunits. These results support a proposed linkage between Brugada syndrome and some instances of sudden infant death and the hypothesis that reduced Na(+) conductance is the primary cause of IVF with STE.


Asunto(s)
Bloqueadores de los Canales de Sodio , Fibrilación Ventricular/metabolismo , Línea Celular , Clonación Molecular , Electrofisiología , Humanos , Cinética , Potenciales de la Membrana , Mutagénesis , Mutación Missense , Técnicas de Placa-Clamp , Canales de Sodio/genética , Temperatura , Transfección , Fibrilación Ventricular/genética
4.
J Mol Cell Cardiol ; 32(10): 1873-84, 2000 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-11013131

RESUMEN

Ventricular fibrillation leading to sudden cardiac death can occur even in the absence of structural heart disease. One form of this so-called idiopathic ventricular fibrillation (IVF) is characterized by ST segment elevation (STE) in the electrocardiogram. Recently we found that IVF with STE is linked to mutations of SCN5A, the gene encoding the cardiac sodium channel alpha -subunit. Two types of defects were identified: loss-of-function mutations that severely truncate channel proteins and missense mutations (e.g. a double mutation, R1232W and T1620M) that cause only minor changes in channel gating. Here we show that co-expression of the R1232W+T1620M missense mutant alpha -subunits in a mammalian cell line stably transfected with human sodium channel beta(1)-subunits results in a phenotype similar to that of the truncation mutants. In the presence of beta(1)subunits the expression of both ionic currents and alpha -subunit-specific, immunoreactive protein was markedly suppressed after transfection of mutant, but not wild-type alpha -subunits when cells were incubated at physiological temperature. Expression was partially restored by incubation at reduced temperatures. Our results reconcile two classes of IVF mutations and support the notion that a reduction in the amplitude of voltage-gated sodium conductance is the primary cause of IVF.


Asunto(s)
Bloqueadores de los Canales de Sodio , Canales de Sodio/genética , Fibrilación Ventricular/metabolismo , Animales , Línea Celular , ADN Complementario/metabolismo , Electrofisiología , Humanos , Immunoblotting , Iones , Cinética , Modelos Biológicos , Mutagénesis Sitio-Dirigida , Mutación Missense , Canal de Sodio Activado por Voltaje NAV1.5 , Oocitos/metabolismo , Fenotipo , Pliegue de Proteína , Estructura Secundaria de Proteína , Estructura Terciaria de Proteína , Canales de Sodio/química , Canales de Sodio/metabolismo , Temperatura , Factores de Tiempo , Transfección , Xenopus/embriología
5.
Circulation ; 101(5): 510-5, 2000 Feb 08.
Artículo en Inglés | MEDLINE | ID: mdl-10662748

RESUMEN

BACKGROUND: A mutation in the cardiac sodium channel gene (SCN5A) has been described in patients with the syndrome of right bundle branch block, ST-segment elevation in leads V1 to V3, and sudden death (Brugada syndrome). These electrocardiographic manifestations are transient in many patients with the syndrome. The present study examined arrhythmic risk in patients with overt and concealed forms of the disease and the effectiveness of sodium channel blockers to unmask the syndrome and, thus, identify patients at risk. METHODS AND RESULTS: The effect of intravenous ajmaline (1 mg/kg), procainamide (10 mg/kg), or flecainide (2 mg/kg) on the ECG was studied in 34 patients with the syndrome and transient normalization of the ECG (group A), 11 members of 3 families in whom a SCN5A mutation was associated with the syndrome and 8 members in whom it was not (group B), and 53 control subjects (group C). Ajmaline, procainamide, or flecainide administration resulted in ST-segment elevation and right bundle branch block in all patients in group A and in all 11 patients with the mutation in group B. A similar pattern could not be elicited in the 8 patients in group B who lacked the mutation or in any person in group C. The follow-up period (37+/-33 months) revealed no differences in the incidence of arrhythmia between the 34 patients in whom the phenotypic manifestation of the syndrome was transient and the 24 patients in whom it was persistent (log-rank, 0.639). CONCLUSIONS: The data demonstrated a similar incidence of potentially lethal arrhythmias in patients displaying transient versus persistent ST-segment elevation and right bundle branch block, as well as the effectiveness of sodium channel blockers to unmask the syndrome and, thus, identify patients at risk.


Asunto(s)
Antiarrítmicos/uso terapéutico , Bloqueo de Rama/complicaciones , Muerte Súbita Cardíaca/etiología , Bloqueadores de los Canales de Sodio , Adulto , Bloqueo de Rama/genética , Electrocardiografía/efectos de los fármacos , Femenino , Estudios de Seguimiento , Humanos , Masculino , Persona de Mediana Edad , Canal de Sodio Activado por Voltaje NAV1.5 , Linaje , Factores de Riesgo , Canales de Sodio/genética
7.
Am J Physiol ; 274(6): C1501-10, 1998 06.
Artículo en Inglés | MEDLINE | ID: mdl-9696692

RESUMEN

We have determined the effects of coexpression of Kv2.1 with electrically silent Kv5.1 or Kv6.1 alpha-subunits in Xenopus oocytes on channel gating. Kv2.1/5.1 selectively accelerated the rate ofinactivation at intermediate potentials (-30 to 0 mV), without affecting the rate at strong depolarization (0 to +40 mV), and markedly accelerated the rate of cumulative inactivation evoked by high-frequency trains of short pulses. Kv5.1 coexpression alsoslowed deactivation of Kv2.1. In contrast, Kv6.1 was much less effective in speeding inactivation at intermediate potentials, had a slowing effect on inactivation at strong depolarizations, and had no effect on cumulative inactivation. Kv6.1, however, had profound effects on activation, including a negative shift of the steady-state activation curve and marked slowing of deactivation tail currents. Support for the notion that the Kv5.1's effects stem from coassembly of alpha-subunits into heteromeric channels was obtained from biochemical evidence of protein-protein interaction and single-channel measurements that showed heterogeneity in unitary conductance. Our results show that Kv5.1 and Kv6.1 function as regulatory alpha-subunits that when coassembled with Kv2.1 can modulate gating in a physiologically relevant manner.


Asunto(s)
Potenciales de Acción/fisiología , Canales de Potasio con Entrada de Voltaje , Canales de Potasio/metabolismo , Canales de Potasio/fisiología , Potenciales de Acción/genética , Animales , Canales de Potasio de Tipo Rectificador Tardío , Expresión Génica , Oocitos/fisiología , Técnicas de Placa-Clamp , Canales de Potasio/genética , Proteínas Recombinantes de Fusión , Canales de Potasio Shab , Transfección , Xenopus
8.
Nature ; 392(6673): 293-6, 1998 Mar 19.
Artículo en Inglés | MEDLINE | ID: mdl-9521325

RESUMEN

Ventricular fibrillation causes more than 300,000 sudden deaths each year in the USA alone. In approximately 5-12% of these cases, there are no demonstrable cardiac or non-cardiac causes to account for the episode, which is therefore classified as idiopathic ventricular fibrillation (IVF). A distinct group of IVF patients has been found to present with a characteristic electrocardiographic pattern. Because of the small size of most pedigrees and the high incidence of sudden death, however, molecular genetic studies of IVF have not yet been done. Because IVF causes cardiac rhythm disturbance, we investigated whether malfunction of ion channels could cause the disorder by studying mutations in the cardiac sodium channel gene SCN5A. We have now identified a missense mutation, a splice-donor mutation, and a frameshift mutation in the coding region of SCN5A in three IVF families. We show that sodium channels with the missense mutation recover from inactivation more rapidly than normal and that the frameshift mutation causes the sodium channel to be non-functional. Our results indicate that mutations in cardiac ion-channel genes contribute to the risk of developing IVF.


Asunto(s)
Mutación , Canales de Sodio/genética , Fibrilación Ventricular/genética , Potenciales de Acción , Animales , Análisis Mutacional de ADN , Electrocardiografía , Electrofisiología , Femenino , Mutación del Sistema de Lectura , Humanos , Activación del Canal Iónico/genética , Cinética , Masculino , Canal de Sodio Activado por Voltaje NAV1.5 , Linaje , Polimorfismo Conformacional Retorcido-Simple , Estructura Secundaria de Proteína , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Canales de Sodio/química , Canales de Sodio/metabolismo , Fibrilación Ventricular/etiología , Fibrilación Ventricular/metabolismo , Xenopus
9.
Biophys J ; 74(4): 1779-89, 1998 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-9545040

RESUMEN

We report here several unusual features of inactivation of the rat Kv2.1 delayed rectifier potassium channel, expressed in Xenopus oocytes. The voltage dependence of inactivation was U-shaped, with maximum inactivation near 0 mV. During a maintained depolarization, development of inactivation was slow and only weakly voltage dependent (tau = 4 s at 0 mV; tau = 7 s at +80 mV). However, recovery from inactivation was strongly voltage dependent (e-fold for 20 mV) and could be rapid (tau = 0.27 s at -140 mV). Kv2.1 showed cumulative inactivation, where inactivation built up during a train of brief depolarizations. A single maintained depolarization produced more steady-state inactivation than a train of pulses, but there could actually be more inactivation with the repeated pulses during the first few seconds. We term this phenomenon "excessive cumulative inactivation." These results can be explained by an allosteric model, in which inactivation is favored by activation of voltage sensors, but the open state of the channel is resistant to inactivation.


Asunto(s)
Modelos Biológicos , Bloqueadores de los Canales de Potasio , Canales de Potasio con Entrada de Voltaje , Canales de Potasio , Regulación Alostérica , Animales , Fenómenos Biofísicos , Biofisica , Canales de Potasio de Tipo Rectificador Tardío , Femenino , Técnicas In Vitro , Cinética , Potenciales de la Membrana , Oocitos/metabolismo , Técnicas de Placa-Clamp , Ratas , Proteínas Recombinantes/antagonistas & inhibidores , Canales de Potasio Shab , Xenopus
10.
Am J Physiol ; 274(2): H477-87, 1998 02.
Artículo en Inglés | MEDLINE | ID: mdl-9486250

RESUMEN

Inherited long Q-T syndrome is a ventricular arrhythmia associated with delayed repolarization and the risk of sudden death. The chromosome 3-linked form of the disease (LQT3) is associated with mutations in the cardiac Na+ channel (N1325S or R1644H; or deletion of residues 1,505-1,507, delta KPQ) that increase late inward currents and may cause delayed repolarization. Late currents arise from dispersed reopenings (N1325S and R1644H) or from reopenings combined with prolonged bursts (delta KPQ). Therefore, we tested whether lidocaine blockade of late current varied among the different LQT3 mutant channels. We found that lidocaine preferentially blocked late over peak current and that the blockade was equally effective in all three channels, expressed in Xenopus oocytes. Lidocaine inhibited both dispersed reopenings and bursting in single channels without affecting mean open times. In the absence of drug, inactivating prepulses inhibited bursting but not dispersed reopenings. We suggest that lidocaine block of late current in LQT3 channels acts via a common mechanism involving stabilization of inactivation. Therefore, blockers that target the inactivated state may be effective therapeutic agents in all three biophysical phenotypes of LQT3.


Asunto(s)
Arritmias Cardíacas/genética , Lidocaína/farmacología , Canales de Sodio/genética , Animales , Antiarrítmicos/farmacología , Cromosomas Humanos Par 3 , Conductividad Eléctrica , Femenino , Eliminación de Gen , Expresión Génica , Ventrículos Cardíacos , Humanos , Mutagénesis Sitio-Dirigida , Mutación , Miocardio/química , Oocitos/metabolismo , Proteínas Recombinantes , Canales de Sodio/efectos de los fármacos , Canales de Sodio/fisiología , Transfección , Xenopus
11.
J Gen Physiol ; 109(6): 767-78, 1997 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-9222902

RESUMEN

The cytoplasmic half of S5 (5'S5) has been identified as part of the inner mouth of the pore based on evidence that mutations in this region greatly alter single channel conductance, 4-aminopyridine (4-AP) block and the rate of channel closing upon repolarization (deactivation). The latter effect, suggestive of a role for 5'S5 in channel gating was investigated in the present study. The biophysical properties of chimeric channels, in which the 5'S5 regions were exchanged between two host channels (Kv2.1 and Kv3.1) that differ in 4-AP sensitivity and deactivation rate, were examined in a Xenopus oocyte expression system. Exchange of 5'S5 between Kv2.1 and Kv3.1 confers steady-state voltage dependence of activation and rates of channel deactivation similar to those of the donor channel. The involvement of voltage-dependent gating was confirmed by the observation that exchanging the 5'S5 segment of Kv2.1 with that of Kv3.1 confers a change from slow to fast deactivation kinetics by accelerating the decay of off-gating charge movement. We suggest that a conformational change that extends from the voltage-sensor in S4 to the region of the pore lined by S5 regulates the stability of the open state. Therefore, the cytoplasmic end of S5, in addition to forming part of the conduction pathway near the inner mouth of the pore, also participates in the conformational rearrangements associated with late steps in channel activation and early steps in deactivation.


Asunto(s)
Proteínas de la Membrana/fisiología , Mutación/genética , Canales de Potasio/fisiología , Animales , Oocitos , Técnicas de Placa-Clamp , Xenopus
12.
J Membr Biol ; 155(1): 11-25, 1997 Jan 01.
Artículo en Inglés | MEDLINE | ID: mdl-9002421

RESUMEN

Aqueous exposure of critical residues in the selectivity region of voltage gated Na+ channels was studied by cysteine-scanning mutagenesis at three positions in each of the SS2 segments of domains III (D3) and IV (D4) of the human heart Na+ channel. Ionic currents were modified by charged cysteine-specific methanethiosulfonate (MTS) reagents, (2-aminoethyl)methanethiosulfonate (MTSEA+) and (2-sulfonatoethyl)methanethiosulfonate (MTSES-) in all six of the Cys-substituted channels, including Trp --> Cys substitutions at homologous positions in D3 and D4 that were predicted in secondary structure models to have buried side chains. Furthermore, in the absence of MTS modification, each of the Cys mutants showed a reduction in tetrodotoxin (TTX) block by a factor >10(2). Cysteine substitution without MTS modification abolished the alkali metal ion selectivity in K1418C (D3), but not in A1720C (the corresponding position in D4) suggesting that the lysine but not the alanine side chains contribute to selectivity even though both were exposed. Neither position responded to MTSES- suggesting that these residues occupy either a size- or charge-restricted region of the pore. By contrast, MTSES- markedly increased, and MTSEA+ markedly decreased conductance of D1713C (D4) suggesting that the acidic side chain of Asp1713 acts electrostatically in an unrestricted region. These results suggest that Lys1418 lies in a restricted region favorable to cations, whereas Asp1713 is at a more peripheral location in the Na+ channel pore.


Asunto(s)
Cisteína/genética , Activación del Canal Iónico , Mutación , Miocardio/metabolismo , Canales de Sodio/metabolismo , Secuencia de Aminoácidos , Proteínas Anfibias , Proteínas Portadoras/efectos de los fármacos , Proteínas Portadoras/metabolismo , Metanosulfonato de Etilo/análogos & derivados , Metanosulfonato de Etilo/farmacología , Humanos , Indicadores y Reactivos , Datos de Secuencia Molecular , Canales de Sodio/efectos de los fármacos
13.
Am J Physiol ; 273(6): C1849-58, 1997 12.
Artículo en Inglés | MEDLINE | ID: mdl-9435489

RESUMEN

Opening and closing of voltage-operated channels requires the interaction of diverse structural elements. One approach to the identification of channel domains that participate in gating is to locate the sites of action of modifiers. Covalent reaction of Kv2.1 channels with the neutral, sulfhydryl-specific methylmethanethiosulfonate (MMTS) caused a slowing of channel gating with a predominant effect on the kinetics of activation. These effects were also obtained after intracellular, but not extracellular, application of a charged MMTS analog. Single channel analysis revealed that MMTS acted primarily by prolonging the latency to first opening without substantially affecting gating transitions after the channel first opens and until it inactivates. To localize the channel cysteine(s) with which MMTS reacts, we generated NH2- and COOH-terminal deletion mutants and a construct in which all three cysteines in transmembrane regions were substituted. Only the NH2-terminal deletion construct gave rise to currents that activated slowly and displayed MMTS-insensitive kinetics. These results show that the NH2-terminal tail of Kv2.1 participates in transitions leading to activation through interactions involving reduced cysteine(s) that can be modulated from the cytoplasmic phase.


Asunto(s)
Canales de Potasio con Entrada de Voltaje , Canales de Potasio/fisiología , Secuencia de Aminoácidos , Sustitución de Aminoácidos , Animales , Canales de Potasio de Tipo Rectificador Tardío , Ditiotreitol/farmacología , Activación del Canal Iónico/efectos de los fármacos , Cinética , Potenciales de la Membrana/efectos de los fármacos , Potenciales de la Membrana/fisiología , Metilmetanosulfonato/análogos & derivados , Metilmetanosulfonato/farmacología , Mutagénesis Insercional , Mutagénesis Sitio-Dirigida , Oocitos/fisiología , Canales de Potasio/biosíntesis , Canales de Potasio/química , Proteínas Recombinantes/biosíntesis , Proteínas Recombinantes/química , Eliminación de Secuencia , Canales de Potasio Shab
14.
FEBS Lett ; 399(1-2): 177-82, 1996 Dec 09.
Artículo en Inglés | MEDLINE | ID: mdl-8980147

RESUMEN

Heteromultimer formation between Kv potassium channel subfamilies with the production of a novel current is reported for the first time. Protein-protein interactions between Kv2.1 and electrically silent Kv6.1 alpha-subunits were detected using two microelectrode voltage clamp and yeast two-hybrid measurements. Amino terminal portions of Kv6.1 were unable to form homomultimers but interacted specifically with amino termini of Kv2.1. Xenopus oocytes co-injected with Kv6.1 and Kv2.1 cRNAs exhibited a novel current with decreased rates of deactivation, decreased sensitivity to TEA block, and a hyperpolarizing shift of the half maximal activation potential when compared to Kv2.1. Our results indicate that Kv channel subfamilies can form heteromultimeric channels and, for the first time, suggest a possible functional role for the Kv6 subfamily.


Asunto(s)
Canales de Potasio/fisiología , Animales , Técnicas de Placa-Clamp , Bloqueadores de los Canales de Potasio , Proteínas Recombinantes de Fusión/fisiología , Canales de Potasio Shab , Tetraetilamonio , Compuestos de Tetraetilamonio/farmacología , Xenopus
15.
Circ Res ; 78(5): 916-24, 1996 May.
Artículo en Inglés | MEDLINE | ID: mdl-8620612

RESUMEN

Inheritable long-QT syndrome (LQTS) is a disease in which delayed ventricular repolarization leads to cardiac arrhythmias and the possibility of sudden death. In the chromosome 3-linked disease, one mutation of the cardiac Na+ channel gene results in a deletion of residues 1505 to 1507 (Delta KPQ), and two mutation result in substitutions (N1325S and R1644H). We compared all three mutant-channel phenotypes by heterologous expression in Xenopus oocytes. Each produced a late phase of inactivation-resistant, mexiletine- and tetrodotoxin-sensitive whole-cell currents, but the underlying mechanisms were different at the single-channel level. N1325S and R1644H showed dispersed reopenings after the initial transient, whereas Delta KPQ showed both dispersed reopenings and long-lasting bursts. Thus, two distinct biophysical defects underlie the in vitro phenotype of persistent current in Na+ channel-linked LQTS, and the additive effects of both are responsible for making the Delta KPQ phenotype the most severe.


Asunto(s)
Síndrome de QT Prolongado/fisiopatología , Canales de Sodio/fisiología , Animales , Conductividad Eléctrica , Activación del Canal Iónico/fisiología , Mutación/fisiología , Oocitos , Fenotipo , Canales de Sodio/genética , Xenopus
16.
Biophys J ; 69(2): 428-34, 1995 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-8527656

RESUMEN

We have mapped residues in the carboxyl half of the P region of a voltage-gated K+ channel that influence external tetraethylammonium (TEA) block. Fifteen amino acids were substituted with cysteine and expressed in oocytes from monomeric or heterodimeric cRNAs. From a total of six mutant channels with altered TEA sensitivity, three were susceptible to modification by extracellularly applied charged methanethiosulfonates (MTSX). Another residue did not affect TEA block but was protected from MTSX by TEA. MTSX modification of position Y380C, thought to form the TEA binding site, affected TEA affinity only moderately, and this effect could be reversed by additional charge transfer from an oppositely charged MTSX analog. The results show that TEA block is modulated from multiple sites, including residues located deep in the pore and that several side chains besides that of Y380 are exposed at the TEA receptor.


Asunto(s)
Bloqueadores de los Canales de Potasio , Compuestos de Tetraetilamonio/farmacología , Secuencia de Aminoácidos , Animales , Sitios de Unión , Fenómenos Biofísicos , Biofisica , Femenino , Potenciales de la Membrana/efectos de los fármacos , Datos de Secuencia Molecular , Mutagénesis Sitio-Dirigida , Oocitos/efectos de los fármacos , Oocitos/metabolismo , Canales de Potasio/genética , Canales de Potasio/metabolismo , Proteínas Recombinantes/antagonistas & inhibidores , Proteínas Recombinantes/genética , Proteínas Recombinantes/metabolismo , Tetraetilamonio , Xenopus laevis
17.
Neuron ; 14(5): 1055-63, 1995 May.
Artículo en Inglés | MEDLINE | ID: mdl-7748553

RESUMEN

The structure of the carboxyl half of the pore-forming region of Kv2.1 was studied by replacing each of 15 consecutive residues between positions 383 and 369 with a reporter cysteine residue. Extracellular application of charged, membrane-impermeant methanethiosulfonates irreversibly modified currents at four cysteine-substituted positions, K382, Y380, I379, and D378. Intracellular exposure to methanethiosulfonate ethyltrimethylammonium revealed another set of reactive mutants (V374, T373, T372, and T370). Our results indicate that positions 378 and 374 are exposed at outer and inner mouths of the channel, respectively, and immersed in the aqueous phase. In contrast to present topological models, the 383-369 region appears to span the pore mainly as a nonperiodic structure.


Asunto(s)
Cisteína/química , Canales de Potasio/química , Secuencia de Aminoácidos , Animales , Secuencia de Bases , Sitios de Unión , Conductividad Eléctrica , Femenino , Expresión Génica , Sustancias Macromoleculares , Mesilatos/farmacología , Datos de Secuencia Molecular , Mutagénesis , Oocitos/metabolismo , Reacción en Cadena de la Polimerasa , Canales de Potasio/genética , Canales de Potasio/fisiología , ARN Complementario/genética , Proteínas Recombinantes , Relación Estructura-Actividad , Tetraetilamonio , Compuestos de Tetraetilamonio/farmacología , Xenopus
18.
Biophys J ; 68(5): 1804-13, 1995 May.
Artículo en Inglés | MEDLINE | ID: mdl-7612822

RESUMEN

Mutation of the glycines in a conserved Gly-Tyr-Gly-Asp sequence in the P-region of voltage-gated K channels has identified determinants of Na/K selectivity. But the function of the negatively charged Asp is not known because mutations at this position are not tolerated, owing to the fourfold replication of mutations in a tetrameric channel. We have successfully mutated Asp378-->Thr in a tandem dimer Kv2.1 construct to yield a twofold neutralization of charge at this site. When expressed in Xenopus oocytes, the mutated channels showed markedly altered ion conduction and blockade. Potassium conduction in the inward direction was selectively reduced, so that the instantaneous current-voltage relationship obtained in isotonic KCl became strongly outwardly rectifying. The relative permeability to Na+, PNa/PK, increased from 0.02 to 0.10 without changing the ion selectivity sequence K > Rb >> Cs >> Na. The IC50 for block by external tetraethylammonium (TEA) increased more than 100-fold without affecting block by internal TEA. We conclude that Asp378 is an essential part of a potassium ion binding site associated with the Na/K selectivity filter at the external mouth of the pore.


Asunto(s)
Ácido Aspártico , Canales de Potasio/química , Canales de Potasio/fisiología , Secuencia de Aminoácidos , Animales , Cationes Monovalentes/metabolismo , Membrana Celular/fisiología , Secuencia Conservada , Femenino , Activación del Canal Iónico/efectos de los fármacos , Activación del Canal Iónico/fisiología , Sustancias Macromoleculares , Datos de Secuencia Molecular , Mutagénesis Sitio-Dirigida , Oocitos/fisiología , Mutación Puntual , Reacción en Cadena de la Polimerasa , Potasio/metabolismo , Canales de Potasio/biosíntesis , Proteínas Recombinantes/biosíntesis , Proteínas Recombinantes/química , Proteínas Recombinantes/metabolismo , Mapeo Restrictivo , Especificidad por Sustrato , Tetraetilamonio , Compuestos de Tetraetilamonio/farmacología , Treonina , Xenopus laevis
19.
Biophys J ; 67(6): 2305-15, 1994 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7696471

RESUMEN

We have probed a cysteine residue that confers resistance to tetrodotoxin (TTX) block in heart Na channels, with membrane-impermeant, cysteine-specific, methanethiosulfonate (MTS) analogs. Covalent addition of a positively charged group to the cysteinyl sulfhydryl reduced pore conductance by 87%. The effect was selectively prevented by treatment with TTX, but not saxitoxin (STX). Addition of a negatively charged group selectively inhibited STX block without affecting TTX block. These results agree with models that place an exposed cysteinyl sulfhydryl in the TTX site adjacent to the mouth of the pore, but do not support the contention that STX and TTX are interchangeable. The surprising differences between the two toxins are consistent with the hypothesis that the toxin-receptor complex can assume different conformations when STX or TTX bound.


Asunto(s)
Saxitoxina/farmacología , Canales de Sodio/efectos de los fármacos , Reactivos de Sulfhidrilo/farmacología , Tetrodotoxina/farmacología , Animales , Fenómenos Biofísicos , Biofisica , Encéfalo/metabolismo , Cisteína/química , Cisteína/genética , ADN Complementario/genética , Electroquímica , Metanosulfonato de Etilo/análogos & derivados , Metanosulfonato de Etilo/farmacología , Femenino , Humanos , Técnicas In Vitro , Conformación Molecular , Miocardio/metabolismo , Mutación Puntual , Saxitoxina/metabolismo , Bloqueadores de los Canales de Sodio , Canales de Sodio/genética , Tetrodotoxina/metabolismo
20.
Biophys J ; 67(6): 2316-25, 1994 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-7696472

RESUMEN

Pore properties that distinguish two cloned, voltage-gated K+ channels, Kv2.1 and Kv3.1, include single-channel conductance, block by external and internal tetraethylammonium, and block by 4-aminopyridine. To define the inner mouth of voltage-gated K+ channels, segmental exchanges and point mutations of nonconserved residues were used. Transplanting the cytoplasmic half of either transmembrane segments S5 or S6 from Kv3.1 into Kv2.1 reduced sensitivity to block by internal tetraethylammonium, increased sensitivity to 4-aminopyridine, and reduced single-channel conductance. In S6, changes in single-channel conductance and internal tetraethylammonium sensitivity were associated with point mutations V400T and L403 M, respectively. Although individual residues in both S5 and S6 were found to affect 4-aminopyridine blockade, the most effective change was L327F in S5. Thus, both S5 and S6 contribute to the inner mouth of the pore but different residues regulate ion conduction and blockade by internal tetraethylammonium and 4-aminopyridine.


Asunto(s)
Mutación , Neuropéptidos , Canales de Potasio con Entrada de Voltaje , Canales de Potasio/genética , Canales de Potasio/metabolismo , 4-Aminopiridina/farmacología , Secuencia de Aminoácidos , Animales , Sitios de Unión/genética , Fenómenos Biofísicos , Biofisica , Canales de Potasio de Tipo Rectificador Tardío , Conductividad Eléctrica , Femenino , Técnicas In Vitro , Datos de Secuencia Molecular , Estructura Molecular , Mutagénesis Sitio-Dirigida , Mutación Puntual , Bloqueadores de los Canales de Potasio , Proteínas Recombinantes de Fusión/antagonistas & inhibidores , Proteínas Recombinantes de Fusión/genética , Proteínas Recombinantes de Fusión/metabolismo , Canales de Potasio Shab , Canales de Potasio Shaw , Tetraetilamonio , Compuestos de Tetraetilamonio/farmacología
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