Literature DB >> 16050261

Voltage sensor movement in the hERG K+ channel.

David R Piper1, Michael C Sanguinetti, Martin Tristani-Firouzi.   

Abstract

The critical role of hERG in the maintenance of normal cardiac electrical activity derives from its unusual gating properties: slow channel activation and fast inactivation. To characterize voltage sensor movement associated with slow activation and fast inactivation, we measured gating currents from wild-type and mutant hERG channels. Fast and slow gating components were observed that differed 100-fold in their kinetics. The slow component constituted the majority of gating charge associated with channel opening and accounted for the sluggish rate of hERG activation. Gating currents from an inactivation-deficient mutant (S631A) were indistinguishable from wild-type, despite a +100 mV shift in the voltage dependence of inactivation, suggesting that a small fraction of total gating charge is devoted to the final transitions that inactivate the channel. Ala-scanning mutagenesis in S4 identified residues that perturbed both charge movement and channel opening. Residues in the S4-S5 linker perturbed channel opening without altering charge displacement, suggesting a role for coupling S4 movement to channel opening. Finally, inactivation-sensitive residues localized to a helical face of S4 adjacent to the activation-sensitive residues. We conclude that S4 acts as the voltage sensor for hERG activation and inactivation and that S4 movement is translated to the activation gate via the S4-S5 linker.

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Year:  2005        PMID: 16050261     DOI: 10.1002/047002142x.ch5

Source DB:  PubMed          Journal:  Novartis Found Symp        ISSN: 1528-2511


  7 in total

1.  Sequence of gating charge movement and pore gating in HERG activation and deactivation pathways.

Authors:  Samuel J Goodchild; Logan C Macdonald; David Fedida
Journal:  Biophys J       Date:  2015-03-24       Impact factor: 4.033

Review 2.  Activation of human ether-a-go-go related gene (hERG) potassium channels by small molecules.

Authors:  Ping-zheng Zhou; Joseph Babcock; Lian-qing Liu; Min Li; Zhao-bing Gao
Journal:  Acta Pharmacol Sin       Date:  2011-05-30       Impact factor: 6.150

Review 3.  Molecular Pathophysiology of Congenital Long QT Syndrome.

Authors:  M S Bohnen; G Peng; S H Robey; C Terrenoire; V Iyer; K J Sampson; R S Kass
Journal:  Physiol Rev       Date:  2017-01       Impact factor: 37.312

Review 4.  The ERG1 K+ Channel and Its Role in Neuronal Health and Disease.

Authors:  Francisco G Sanchez-Conde; Eric N Jimenez-Vazquez; David S Auerbach; David K Jones
Journal:  Front Mol Neurosci       Date:  2022-05-03       Impact factor: 6.261

5.  The hERG K(+) channel S4 domain L532P mutation: characterization at 37°C.

Authors:  Yi H Zhang; Charlotte K Colenso; Richard B Sessions; Christopher E Dempsey; Jules C Hancox
Journal:  Biochim Biophys Acta       Date:  2011-07-14

6.  Hysteretic hERG channel gating current recorded at physiological temperature.

Authors:  David K Jones
Journal:  Sci Rep       Date:  2022-04-08       Impact factor: 4.379

7.  Mechanism of electromechanical coupling in voltage-gated potassium channels.

Authors:  Rikard Blunck; Zarah Batulan
Journal:  Front Pharmacol       Date:  2012-09-12       Impact factor: 5.810

  7 in total

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