Literature DB >> 11325723

Inwardly rectifying current-voltage relationship of small-conductance Ca2+-activated K+ channels rendered by intracellular divalent cation blockade.

H Soh1, C S Park.   

Abstract

Small conductance Ca2+-activated K+ channels (SK(Ca) channels) are a group of K+-selective ion channels activated by submicromolar concentrations of intracellular Ca2+ independent of membrane voltages. We expressed a cloned SK(Ca) channel, rSK2, in Xenopus oocytes and investigated the effects of intracellular divalent cations on the current-voltage (I-V) relationship of the channels. Both Mg2+ and Ca2+ reduced the rSK2 channel currents in voltage-dependent manners from the intracellular side and thus rectified the I-V relationship at physiological concentration ranges. The apparent affinity of Mg2+ was changed as a function of both transmembrane voltage and intracellular Ca2+ concentration. Extracellular K+ altered the voltage dependence as well as the apparent affinities of Mg2+ binding from intracellular side. Thus, the inwardly rectifying I-V relationship of SK(Ca) channels is likely due to the voltage-dependent blockade of intracellular divalent cations and that the binding site is located within the ion-conducting pathway. Therefore, intracellular Ca2+ modulates the permeation characteristics of SK(Ca) channels by altering the I-V relationship as well as activates the channel by interacting with the gating machinery, calmodulin, and SK(Ca) channels can be considered as Ca2+-activated inward rectifier K+ channels.

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Year:  2001        PMID: 11325723      PMCID: PMC1301412          DOI: 10.1016/S0006-3495(01)76193-0

Source DB:  PubMed          Journal:  Biophys J        ISSN: 0006-3495            Impact factor:   4.033


  19 in total

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Authors:  C M ARMSTRONG; L BINSTOCK
Journal:  J Gen Physiol       Date:  1965-05       Impact factor: 4.086

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  26 in total

1.  Localization of divalent cation-binding site in the pore of a small conductance Ca(2+)-activated K(+) channel and its role in determining current-voltage relationship.

Authors:  Heun Soh; Chul-Seung Park
Journal:  Biophys J       Date:  2002-11       Impact factor: 4.033

2.  Functional effects of auxiliary beta4-subunit on rat large-conductance Ca(2+)-activated K(+) channel.

Authors:  Tal Soo Ha; Moon-Sun Heo; Chul-Seung Park
Journal:  Biophys J       Date:  2004-05       Impact factor: 4.033

3.  Cloning and characterization of SK2 channel from chicken short hair cells.

Authors:  T M Matthews; R K Duncan; M Zidanic; T H Michael; P A Fuchs
Journal:  J Comp Physiol A Neuroethol Sens Neural Behav Physiol       Date:  2005-05-03       Impact factor: 1.836

4.  Sodium permeability of a cloned small-conductance calcium-activated potassium channel.

Authors:  Narae Shin; Heun Soh; Sunghoe Chang; Do Han Kim; Chul-Seung Park
Journal:  Biophys J       Date:  2005-09-02       Impact factor: 4.033

Review 5.  K+ channels in apoptosis.

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6.  Functional reduction of SK3-mediated currents precedes AMPA-receptor-mediated excitotoxicity in dopaminergic neurons.

Authors:  Bruno A Benítez; Helen M Belálcazar; Agustín Anastasía; Daniel T Mamah; Charles F Zorumski; Daniel H Mascó; Daniel G Herrera; Gabriel A de Erausquin
Journal:  Neuropharmacology       Date:  2010-10-31       Impact factor: 5.250

7.  Electrostatic influences of charged inner pore residues on the conductance and gating of small conductance Ca2+ activated K+ channels.

Authors:  Weiyan Li; Richard W Aldrich
Journal:  Proc Natl Acad Sci U S A       Date:  2011-03-21       Impact factor: 11.205

8.  Activation of the SK potassium channel-calmodulin complex by nanomolar concentrations of terbium.

Authors:  Weiyan Li; Richard W Aldrich
Journal:  Proc Natl Acad Sci U S A       Date:  2009-01-14       Impact factor: 11.205

9.  EF hands at the N-lobe of calmodulin are required for both SK channel gating and stable SK-calmodulin interaction.

Authors:  Weiyan Li; David B Halling; Amelia W Hall; Richard W Aldrich
Journal:  J Gen Physiol       Date:  2009-09-14       Impact factor: 4.086

10.  Inhibition of K(Ca)2.2 and K(Ca)2.3 channel currents by protonation of outer pore histidine residues.

Authors:  Samuel J Goodchild; Cedric Lamy; Vincent Seutin; Neil V Marrion
Journal:  J Gen Physiol       Date:  2009-10       Impact factor: 4.086

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