Literature DB >> 10551270

Characterization of human Kv4.2 mediating a rapidly-inactivating transient voltage-sensitive K+ current.

X R Zhu1, A Wulf, M Schwarz, D Isbrandt, O Pongs.   

Abstract

A human cDNA for the voltage-sensitive potassium channel subunit Kv4.2 has been cloned and functionally characterized. The human Kv4.2 (KCND2) gene was mapped at 7q31-32. Kv4.2 mRNA is prominently expressed in human brain. Relatively high concentrations of Kv4.2 mRNA occurred in mRNA preparations of amygdala, caudate nucleus, cerebellum, hippocampus, substantia nigra, and thalamus. Kv4.2 mRNA was not detected in human heart, kidney, liver, lung, pancreas, and skeletal muscle. The derived Kv4.2 open reading frame consists of 630 amino acids. In comparison to rat Kv4.2, the human Kv4.2 sequence is highly conserved showing amino acid sequence differences at five positions only. The Kv4.2 subunits were expressed heterologously in human embryonic kidney (293) cells and mediated a rapidly inactivating, A-type outward K+ current. The gating kinetics of the Kv4.2-mediated currents were very similar to those of rat Kv4.2-mediated currents. Both the Kv4.2 and Kv4.3 subunits have been implicated in mediating the transient outward K+ current Ito in rodent cardiac myocytes. In contrast we did not detect Kv4.2. but solely Kv4.3 mRNA in human heart RNA preparations. This may suggest that Kv4.2 subunits do not contribute to the rapid transient outward K+ current of atrial and ventricular myocytes in humans.

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Year:  1999        PMID: 10551270

Source DB:  PubMed          Journal:  Receptors Channels        ISSN: 1060-6823


  24 in total

1.  Solution structure of hpTX2, a toxin from Heteropoda venatoria spider that blocks Kv4.2 potassium channel.

Authors:  C Bernard; C Legros; G Ferrat; U Bischoff; A Marquardt; O Pongs; H Darbon
Journal:  Protein Sci       Date:  2000-11       Impact factor: 6.725

2.  Kinetic analysis of open- and closed-state inactivation transitions in human Kv4.2 A-type potassium channels.

Authors:  R Bähring; L M Boland; A Varghese; M Gebauer; O Pongs
Journal:  J Physiol       Date:  2001-08-15       Impact factor: 5.182

3.  N-type inactivation features of Kv4.2 channel gating.

Authors:  Manuel Gebauer; Dirk Isbrandt; Kathrin Sauter; Britta Callsen; Andreas Nolting; Olaf Pongs; Robert Bähring
Journal:  Biophys J       Date:  2004-01       Impact factor: 4.033

4.  Co-assembly of Kv4 {alpha} subunits with K+ channel-interacting protein 2 stabilizes protein expression and promotes surface retention of channel complexes.

Authors:  Nicholas C Foeger; Céline Marionneau; Jeanne M Nerbonne
Journal:  J Biol Chem       Date:  2010-08-13       Impact factor: 5.157

5.  Intra- and Intersubunit Dynamic Binding in Kv4.2 Channel Closed-State Inactivation.

Authors:  Jessica Wollberg; Robert Bähring
Journal:  Biophys J       Date:  2016-01-05       Impact factor: 4.033

6.  Contribution of N- and C-terminal Kv4.2 channel domains to KChIP interaction [corrected].

Authors:  Britta Callsen; Dirk Isbrandt; Kathrin Sauter; L Sven Hartmann; Olaf Pongs; Robert Bähring
Journal:  J Physiol       Date:  2005-08-11       Impact factor: 5.182

7.  Augmentation of Kv4.2-encoded currents by accessory dipeptidyl peptidase 6 and 10 subunits reflects selective cell surface Kv4.2 protein stabilization.

Authors:  Nicholas C Foeger; Aaron J Norris; Lisa M Wren; Jeanne M Nerbonne
Journal:  J Biol Chem       Date:  2012-02-06       Impact factor: 5.157

8.  Role of N-terminal domain and accessory subunits in controlling deactivation-inactivation coupling of Kv4.2 channels.

Authors:  Jan Barghaan; Magdalini Tozakidou; Heimo Ehmke; Robert Bähring
Journal:  Biophys J       Date:  2007-11-02       Impact factor: 4.033

Review 9.  Ion Channels in the Heart.

Authors:  Daniel C Bartos; Eleonora Grandi; Crystal M Ripplinger
Journal:  Compr Physiol       Date:  2015-07-01       Impact factor: 9.090

Review 10.  Transmural gradients in ion channel and auxiliary subunit expression.

Authors:  David McKinnon; Barbara Rosati
Journal:  Prog Biophys Mol Biol       Date:  2016-10-01       Impact factor: 3.667

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