Literature DB >> 15452196

New insights on the voltage dependence of the KCa3.1 channel block by internal TBA.

Umberto Banderali1, Hélène Klein, Line Garneau, Manuel Simoes, Lucie Parent, Rémy Sauvé.   

Abstract

We present in this work a structural model of the open IKCa (KCa3.1) channel derived by homology modeling from the MthK channel structure, and used this model to compute the transmembrane potential profile along the channel pore. This analysis showed that the selectivity filter and the region extending from the channel inner cavity to the internal medium should respectively account for 81% and 16% of the transmembrane potential difference. We found however that the voltage dependence of the IKCa block by the quaternary ammonium ion TBA applied internally is compatible with an apparent electrical distance delta of 0.49 +/- 0.02 (n = 6) for negative potentials. To reconcile this observation with the electrostatic potential profile predicted for the channel pore, we modeled the IKCa block by TBA assuming that the voltage dependence of the block is governed by both the difference in potential between the channel cavity and the internal medium, and the potential profile along the selectivity filter region through an effect on the filter ion occupancy states. The resulting model predicts that delta should be voltage dependent, being larger at negative than positive potentials. The model also indicates that raising the internal K+ concentration should decrease the value of delta measured at negative potentials independently of the external K+ concentration, whereas raising the external K+ concentration should minimally affect delta for concentrations >50 mM. All these predictions are born out by our current experimental results. Finally, we found that the substitutions V275C and V275A increased the voltage sensitivity of the TBA block, suggesting that TBA could move further into the pore, thus leading to stronger interactions between TBA and the ions in the selectivity filter. Globally, these results support a model whereby the voltage dependence of the TBA block in IKCa is mainly governed by the voltage dependence of the ion occupancy states of the selectivity filter.

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Year:  2004        PMID: 15452196      PMCID: PMC2233899          DOI: 10.1085/jgp.200409145

Source DB:  PubMed          Journal:  J Gen Physiol        ISSN: 0022-1295            Impact factor:   4.086


  45 in total

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2.  Comparative protein modelling by satisfaction of spatial restraints.

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6.  The internal quaternary ammonium receptor site of Shaker potassium channels.

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7.  Small-conductance, calcium-activated potassium channels from mammalian brain.

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8.  Probing a Ca2+-activated K+ channel with quaternary ammonium ions.

Authors:  A Villarroel; O Alvarez; A Oberhauser; R Latorre
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9.  Analysis of a novel double-barreled anion channel from rat liver rough endoplasmic reticulum.

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Journal:  J Gen Physiol       Date:  2007-03-12       Impact factor: 4.086

4.  Characterizing the fatty acid binding site in the cavity of potassium channel KcsA.

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5.  Contribution of the KCa3.1 channel-calmodulin interactions to the regulation of the KCa3.1 gating process.

Authors:  Patricia Morales; Line Garneau; Hélène Klein; Marie-France Lavoie; Lucie Parent; Rémy Sauvé
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Journal:  J Gen Physiol       Date:  2014-02       Impact factor: 4.086

  6 in total

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