Click here to close
Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly.
We suggest using a current version of Chrome,
FireFox, or Safari.
Modulation of 4-AP block of a mammalian A-type K channel clone by channel gating and membrane voltage.
Yao JA
,
Tseng GN
.
???displayArticle.abstract???
We examined the state-, voltage-, and time dependences of interaction between 4-AP and a mammalian A-type K channel clone (rKv1.4) expressed in Xenopus oocytes using whole-cell and single-channel recordings. 4-AP blocked rKv1.4 from the cytoplasmic side of the membrane. The development of block required channel opening. Block was potentiated by removing the fast inactivation gate of the channel (deletion mutant termed "Del A"). A short-pulse train that activated rKv1.4 without inactivation induced more block by 4-AP than a long pulse that activated and then inactivated the channel. These observations suggest that both activation and inactivation gates limit the binding of 4-AP to the channel. Unblock of 4-AP also occurred during channel opening, because unblock required depolarization and was accelerated by more frequent or longer depolarization pulses (use-dependent unblock). Analysis of the concentration dependence of rate of block development indicated that 4-AP blocked rKv1.4 with slow kinetics (at -20 mV, binding and unbinding rate constants were 3.2 mM-1 s-1 and 4.3 s-1). This was consistent with single-channel recordings: 4-AP induced little or no changes in the fast kinetics of opening and closing within bursts, but shortened the mean burst duration and, more importantly, reduced the probability of channel opening by depolarization. Depolarization might decrease the affinity of 4-AP binding site in the open channel, because stronger depolarization reduced the degree of steady-state block by 4-AP. Furthermore, after 4-AP block had been established at a depolarized holding voltage, further depolarization induced a time-dependent unblock. Our data suggest that 4-AP binds to and unbinds from open rKv1.4 channels with slow kinetics, with the binding site accessibility controlled by the channel gating apparatus and binding site affinity modulated by membrane voltage.
Arhem,
A model for the fast 4-aminopyridine effects on amphibian myelinated nerve fibres. A study based on voltage-clamp experiments.
1989, Pubmed,
Xenbase
Arhem,
A model for the fast 4-aminopyridine effects on amphibian myelinated nerve fibres. A study based on voltage-clamp experiments.
1989,
Pubmed
,
Xenbase
Baldwin,
Characterization of a mammalian cDNA for an inactivating voltage-sensitive K+ channel.
1991,
Pubmed
,
Xenbase
Blair,
Functional characterization of RK5, a voltage-gated K+ channel cloned from the rat cardiovascular system.
1991,
Pubmed
,
Xenbase
Boton,
Two calcium-activated chloride conductances in Xenopus laevis oocytes permeabilized with the ionophore A23187.
1989,
Pubmed
,
Xenbase
Campbell,
The calcium-independent transient outward potassium current in isolated ferret right ventricular myocytes. II. Closed state reverse use-dependent block by 4-aminopyridine.
1993,
Pubmed
Castle,
Characterization of 4-aminopyridine block of the transient outward K+ current in adult rat ventricular myocytes.
1993,
Pubmed
Choquet,
Mechanism of 4-aminopyridine action on voltage-gated potassium channels in lymphocytes.
1992,
Pubmed
Colatsky,
Channel specificity in antiarrhythmic drug action. Mechanism of potassium channel block and its role in suppressing and aggravating cardiac arrhythmias.
1990,
Pubmed
Davies,
The flickery block of ATP-dependent potassium channels of skeletal muscle by internal 4-aminopyridine.
1991,
Pubmed
Duan,
Potassium channel blocking properties of propafenone in rabbit atrial myocytes.
1993,
Pubmed
Hamill,
Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches.
1981,
Pubmed
Kehl,
4-Aminopyridine causes a voltage-dependent block of the transient outward K+ current in rat melanotrophs.
1990,
Pubmed
Kirsch,
Modulation of aminopyridine block of potassium currents in squid axon.
1986,
Pubmed
Kirsch,
Site of action and active form of aminopyridines in squid axon membranes.
1983,
Pubmed
Kirsch,
Gating-dependent mechanism of 4-aminopyridine block in two related potassium channels.
1993,
Pubmed
,
Xenbase
Kirsch,
Segmental exchanges define 4-aminopyridine binding and the inner mouth of K+ pores.
1993,
Pubmed
Liman,
Voltage-sensing residues in the S4 region of a mammalian K+ channel.
1991,
Pubmed
,
Xenbase
Magleby,
Burst kinetics of single calcium-activated potassium channels in cultured rat muscle.
1983,
Pubmed
McCormack,
A role for hydrophobic residues in the voltage-dependent gating of Shaker K+ channels.
1991,
Pubmed
,
Xenbase
McCormack,
A characterization of the activating structural rearrangements in voltage-dependent Shaker K+ channels.
1994,
Pubmed
Methfessel,
Patch clamp measurements on Xenopus laevis oocytes: currents through endogenous channels and implanted acetylcholine receptor and sodium channels.
1986,
Pubmed
,
Xenbase
Papazian,
Alteration of voltage-dependence of Shaker potassium channel by mutations in the S4 sequence.
1991,
Pubmed
,
Xenbase
Po,
Heteromultimeric assembly of human potassium channels. Molecular basis of a transient outward current?
1993,
Pubmed
,
Xenbase
Schoppa,
The size of gating charge in wild-type and mutant Shaker potassium channels.
1992,
Pubmed
Simurda,
Use-dependent effects of 4-aminopyridine on transient outward current in dog ventricular muscle.
1989,
Pubmed
Snyders,
Time-, voltage-, and state-dependent block by quinidine of a cloned human cardiac potassium channel.
1992,
Pubmed
Thompson,
Aminopyridine block of transient potassium current.
1982,
Pubmed
Tseng,
Differential effects of elevating [K]o on three transient outward potassium channels. Dependence on channel inactivation mechanisms.
1992,
Pubmed
,
Xenbase
Tseng-Crank,
Functional role of the NH2-terminal cytoplasmic domain of a mammalian A-type K channel.
1993,
Pubmed
,
Xenbase
Tseng-Crank,
Molecular cloning and functional expression of a potassium channel cDNA isolated from a rat cardiac library.
1990,
Pubmed
,
Xenbase
Wagoner,
Aminopyridines block an inactivating potassium current having slow recovery kinetics.
1990,
Pubmed
Welling,
Subunit-dependent modulation of recombinant L-type calcium channels. Molecular basis for dihydropyridine tissue selectivity.
1993,
Pubmed
Woodhull,
Ionic blockage of sodium channels in nerve.
1973,
Pubmed
Yeh,
Dynamics of aminopyridine block of potassium channels in squid axon membrane.
1976,
Pubmed
Zagotta,
Voltage-dependent gating of Shaker A-type potassium channels in Drosophila muscle.
1990,
Pubmed