Literature DB >> 8788936

C-type inactivation controls recovery in a fast inactivating cardiac K+ channel (Kv1.4) expressed in Xenopus oocytes.

R L Rasmusson1, M J Morales, R C Castellino, Y Zhang, D L Campbell, H C Strauss.   

Abstract

1. A fast inactivating transient K+ current (FK1) cloned from ferret ventricle and expressed in Xenopus oocytes was studied using the two-electrode voltage clamp technique. Removal of the NH2-terminal domain of FK1 (FK1 delta 2-146) removed fast inactivation consistent with previous findings in Kv1.4 channels. The NH2-terminal deletion mutation revealed a slow inactivation process, which matches the criteria for C-type inactivation described for Shaker B channels. 2. Inactivation of FK1 delta 2-146 at depolarized potentials was well described by a single exponential process with a voltage-insensitive time constant. In the range -90 to +20 mV, steady-state C-type inactivation was well described by a Boltzmann relationship that compares closely with inactivation measured in the presence of the NH2-terminus. These results suggest that C-type inactivation is coupled to activation. 3. The coupling of C-type inactivation to activation was assessed by mutation of the fourth positively charged residue (arginine 454) in the S4 voltage sensor to glutamine (R454Q). This mutation produced a hyperpolarizing shift in the inactivation relationship of both FK1 and FK1 delta 2-146 without altering the rate of inactivation of either clone. 4. The rates of recovery from inactivation are nearly identical in FK1 and FK1 delta 2-146. 5. To assess the mechanisms underlying recovery from inactivation the effects of elevated [K+]o and selective mutations in the extracellular pore and the S4 voltage sensor were compared in FK1 and FK1 delta 2-146. The similarity in recovery rates in response to these perturbations suggests that recovery from C-type inactivation governs the overall rate of recovery of inactivated channels for both FK1 and FK1 delta 2-146. 6. Analysis of the rate of recovery of FK1 channels for inactivating pulses of different durations (70-2000 ms) indicates that recovery rate is insensitive to the duration of the inactivating pulse.

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Year:  1995        PMID: 8788936      PMCID: PMC1156841          DOI: 10.1113/jphysiol.1995.sp021085

Source DB:  PubMed          Journal:  J Physiol        ISSN: 0022-3751            Impact factor:   5.182


  19 in total

1.  Restoration of inactivation in mutants of Shaker potassium channels by a peptide derived from ShB.

Authors:  W N Zagotta; T Hoshi; R W Aldrich
Journal:  Science       Date:  1990-10-26       Impact factor: 47.728

2.  Biophysical and molecular mechanisms of Shaker potassium channel inactivation.

Authors:  T Hoshi; W N Zagotta; R W Aldrich
Journal:  Science       Date:  1990-10-26       Impact factor: 47.728

3.  Ion channels. Not an open-and-shut case.

Authors:  S W Jones
Journal:  Nature       Date:  1991-10-17       Impact factor: 49.962

4.  Alteration of voltage-dependence of Shaker potassium channel by mutations in the S4 sequence.

Authors:  D M Papazian; L C Timpe; Y N Jan; L Y Jan
Journal:  Nature       Date:  1991-01-24       Impact factor: 49.962

5.  Two types of inactivation in Shaker K+ channels: effects of alterations in the carboxy-terminal region.

Authors:  T Hoshi; W N Zagotta; R W Aldrich
Journal:  Neuron       Date:  1991-10       Impact factor: 17.173

6.  Current inactivation involves a histidine residue in the pore of the rat lymphocyte potassium channel RGK5.

Authors:  A E Busch; R S Hurst; R A North; J P Adelman; M P Kavanaugh
Journal:  Biochem Biophys Res Commun       Date:  1991-09-30       Impact factor: 3.575

7.  Regulation of fast inactivation of cloned mammalian IK(A) channels by cysteine oxidation.

Authors:  J P Ruppersberg; M Stocker; O Pongs; S H Heinemann; R Frank; M Koenen
Journal:  Nature       Date:  1991-08-22       Impact factor: 49.962

8.  Tetraethylammonium blockade distinguishes two inactivation mechanisms in voltage-activated K+ channels.

Authors:  K L Choi; R W Aldrich; G Yellen
Journal:  Proc Natl Acad Sci U S A       Date:  1991-06-15       Impact factor: 11.205

9.  Block by 4-aminopyridine of a Kv1.2 delayed rectifier K+ current expressed in Xenopus oocytes.

Authors:  S N Russell; N G Publicover; P J Hart; A Carl; J R Hume; K M Sanders; B Horowitz
Journal:  J Physiol       Date:  1994-12-15       Impact factor: 5.182

10.  Interaction of tetraethylammonium ion derivatives with the potassium channels of giant axons.

Authors:  C M Armstrong
Journal:  J Gen Physiol       Date:  1971-10       Impact factor: 4.086

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  55 in total

1.  U-type inactivation of Kv3.1 and Shaker potassium channels.

Authors:  K G Klemic; G E Kirsch; S W Jones
Journal:  Biophys J       Date:  2001-08       Impact factor: 4.033

2.  Inactivation and recovery in Kv1.4 K+ channels: lipophilic interactions at the intracellular mouth of the pore.

Authors:  Glenna C L Bett; Randall L Rasmusson
Journal:  J Physiol       Date:  2003-11-07       Impact factor: 5.182

3.  C-type inactivation involves a significant decrease in the intracellular aqueous pore volume of Kv1.4 K+ channels expressed in Xenopus oocytes.

Authors:  XueJun Jiang; Glenna C L Bett; XiaoYan Li; Vladimir E Bondarenko; Randall L Rasmusson
Journal:  J Physiol       Date:  2003-05-02       Impact factor: 5.182

4.  Regulation of Kv4.3 voltage-dependent gating kinetics by KChIP2 isoforms.

Authors:  Sangita P Patel; Rajarshi Parai; Rita Parai; Donald L Campbell
Journal:  J Physiol       Date:  2004-01-14       Impact factor: 5.182

5.  Kv1.4 channel block by quinidine: evidence for a drug-induced allosteric effect.

Authors:  Shimin Wang; Michael J Morales; Yu-Jie Qu; Glenna C L Bett; Harold C Strauss; Randall L Rasmusson
Journal:  J Physiol       Date:  2003-01-15       Impact factor: 5.182

6.  Activation properties of Kv4.3 channels: time, voltage and [K+]o dependence.

Authors:  Shimin Wang; Vladimir E Bondarenko; Yujie Qu; Michael J Morales; Randall L Rasmusson; Harold C Strauss
Journal:  J Physiol       Date:  2004-03-05       Impact factor: 5.182

7.  K(V)4.3 N-terminal deletion mutant Δ2-39: effects on inactivation and recovery characteristics in both the absence and presence of KChIP2b.

Authors:  Laura J Hovind; Matthew R Skerritt; Donald L Campbell
Journal:  Channels (Austin)       Date:  2011-01-01       Impact factor: 2.581

8.  A model of the interaction between N-type and C-type inactivation in Kv1.4 channels.

Authors:  Glenna C L Bett; Isidore Dinga-Madou; Qinlian Zhou; Vladimir E Bondarenko; Randall L Rasmusson
Journal:  Biophys J       Date:  2011-01-05       Impact factor: 4.033

9.  Extracellular potassium effects are conserved within the rat erg K+ channel family.

Authors:  Patrick Sturm; Sönke Wimmers; Jürgen R Schwarz; Christiane K Bauer
Journal:  J Physiol       Date:  2005-02-10       Impact factor: 5.182

10.  Imipramine inhibition of transient K+ current: an external open channel blocker preventing fast inactivation.

Authors:  C C Kuo
Journal:  Biophys J       Date:  1998-12       Impact factor: 4.033

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