Literature DB >> 25063820

Cooperative subunit interactions mediate fast C-type inactivation of hERG1 K+ channels.

Wei Wu1, Alison Gardner1, Michael C Sanguinetti2.   

Abstract

At depolarized membrane potentials, the conductance of some voltage-gated K(+) channels is reduced by C-type inactivation. This gating process is voltage independent in Kv1 and involves a conformational change in the selectivity filter that is mediated by cooperative subunit interactions. C-type inactivation in hERG1 K(+) channels is voltage-dependent, much faster in onset and greatly attenuates currents at positive potentials. Here we investigate the potential role of subunit interactions in C-type inactivation of hERG1 channels. Point mutations in hERG1 known to eliminate (G628C/S631C), inhibit (S620T or S631A) or enhance (T618A or M645C) C-type inactivation were introduced into subunits that were combined with wild-type subunits to form concatenated tetrameric channels with defined subunit composition and stoichiometry. Channels were heterologously expressed in Xenopus oocytes and the two-microelectrode voltage clamp was used to measure the kinetics and steady-state properties of inactivation of whole cell currents. The effect of S631A or T618A mutations on inactivation was a graded function of the number of mutant subunits within a concatenated tetramer as predicted by a sequential model of cooperative subunit interactions, whereas M645C subunits increased the rate of inactivation of concatemers, as predicted for subunits that act independently of one another. For mutations located within the inactivation gate proper (S620T or G628C/S631C), the presence of a single subunit in a concatenated hERG1 tetramer disrupted gating to the same extent as that observed for mutant homotetramers. Together, our findings indicate that the final step of C-type inactivation of hERG1 channels involves a concerted, all-or-none cooperative interaction between all four subunits, and that probing the mechanisms of channel gating with concatenated heterotypic channels should be interpreted with care, as conclusions regarding the nature of subunit interactions may depend on the specific mutation used to probe the gating process.
© 2014 The Authors. The Journal of Physiology © 2014 The Physiological Society.

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Year:  2014        PMID: 25063820      PMCID: PMC4287738          DOI: 10.1113/jphysiol.2014.277483

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


  46 in total

1.  Potassium channel receptor site for the inactivation gate and quaternary amine inhibitors.

Authors:  M Zhou; J H Morais-Cabral; S Mann; R MacKinnon
Journal:  Nature       Date:  2001-06-07       Impact factor: 49.962

Review 2.  Ion channels: does each subunit do something on its own?

Authors:  Jeffrey W Karpen; MariaLuisa Ruiz
Journal:  Trends Biochem Sci       Date:  2002-08       Impact factor: 13.807

3.  Semisynthetic K+ channels show that the constricted conformation of the selectivity filter is not the C-type inactivated state.

Authors:  Prasanna K Devaraneni; Alexander G Komarov; Corey A Costantino; Jordan J Devereaux; Kimberly Matulef; Francis I Valiyaveetil
Journal:  Proc Natl Acad Sci U S A       Date:  2013-09-09       Impact factor: 11.205

4.  Pore helices play a dynamic role as integrators of domain motion during Kv11.1 channel inactivation gating.

Authors:  Matthew D Perry; Chai Ann Ng; Jamie I Vandenberg
Journal:  J Biol Chem       Date:  2013-03-07       Impact factor: 5.157

5.  Molecular determinants for activation of human ether-à-go-go-related gene 1 potassium channels by 3-nitro-n-(4-phenoxyphenyl) benzamide.

Authors:  Vivek Garg; Anna Stary-Weinzinger; Frank Sachse; Michael C Sanguinetti
Journal:  Mol Pharmacol       Date:  2011-07-08       Impact factor: 4.436

6.  Molecular coupling in the human ether-a-go-go-related gene-1 (hERG1) K+ channel inactivation pathway.

Authors:  Tania Ferrer; Julio F Cordero-Morales; Marcelo Arias; Eckhard Ficker; David Medovoy; Eduardo Perozo; Martin Tristani-Firouzi
Journal:  J Biol Chem       Date:  2011-09-09       Impact factor: 5.157

7.  C-type inactivation of voltage-gated K+ channels: pore constriction or dilation?

Authors:  Toshinori Hoshi; Clay M Armstrong
Journal:  J Gen Physiol       Date:  2013-01-14       Impact factor: 4.086

8.  Independence and cooperativity in rearrangements of a potassium channel voltage sensor revealed by single subunit fluorescence.

Authors:  L M Mannuzzu; E Y Isacoff
Journal:  J Gen Physiol       Date:  2000-03       Impact factor: 4.086

9.  Stoichiometry of altered hERG1 channel gating by small molecule activators.

Authors:  Wei Wu; Frank B Sachse; Alison Gardner; Michael C Sanguinetti
Journal:  J Gen Physiol       Date:  2014-03-17       Impact factor: 4.086

10.  Hydrophobic interactions between the voltage sensor and pore mediate inactivation in Kv11.1 channels.

Authors:  Matthew D Perry; Sophia Wong; Chai Ann Ng; Jamie I Vandenberg
Journal:  J Gen Physiol       Date:  2013-09       Impact factor: 4.086

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  12 in total

1.  The Link between Inactivation and High-Affinity Block of hERG1 Channels.

Authors:  Wei Wu; Alison Gardner; Michael C Sanguinetti
Journal:  Mol Pharmacol       Date:  2015-04-08       Impact factor: 4.436

2.  Concatenated hERG1 tetramers reveal stoichiometry of altered channel gating by RPR-260243.

Authors:  Wei Wu; Alison Gardner; Michael C Sanguinetti
Journal:  Mol Pharmacol       Date:  2014-12-17       Impact factor: 4.436

3.  Can many subunits make light work of ion channel inactivation?

Authors:  Jamie I Vandenberg; Matthew D Perry
Journal:  J Physiol       Date:  2014-10-15       Impact factor: 5.182

Review 4.  Getting to the heart of hERG K(+) channel gating.

Authors:  Matthew D Perry; Chai-Ann Ng; Stefan A Mann; Arash Sadrieh; Mohammad Imtiaz; Adam P Hill; Jamie I Vandenberg
Journal:  J Physiol       Date:  2015-06-15       Impact factor: 5.182

5.  The Pore-Lipid Interface: Role of Amino-Acid Determinants of Lipophilic Access by Ivabradine to the hERG1 Pore Domain.

Authors:  Laura Perissinotti; Jiqing Guo; Meruyert Kudaibergenova; James Lees-Miller; Marina Ol'khovich; Angelica Sharapova; German L Perlovich; Daniel A Muruve; Brenda Gerull; Sergei Yu Noskov; Henry J Duff
Journal:  Mol Pharmacol       Date:  2019-06-10       Impact factor: 4.436

6.  Rescue of protein expression defects may not be enough to abolish the pro-arrhythmic phenotype of long QT type 2 mutations.

Authors:  Matthew D Perry; Chai Ann Ng; Kevin Phan; Erikka David; Kieran Steer; Mark J Hunter; Stefan A Mann; Mohammad Imtiaz; Adam P Hill; Ying Ke; Jamie I Vandenberg
Journal:  J Physiol       Date:  2016-05-27       Impact factor: 5.182

Review 7.  Molecular Basis of Cardiac Delayed Rectifier Potassium Channel Function and Pharmacology.

Authors:  Wei Wu; Michael C Sanguinetti
Journal:  Card Electrophysiol Clin       Date:  2016-03-18

Review 8.  Ether-à-go-go K+ channels: effective modulators of neuronal excitability.

Authors:  Christiane K Bauer; Jürgen R Schwarz
Journal:  J Physiol       Date:  2018-02-06       Impact factor: 5.182

9.  Intersubunit Concerted Cooperative and cis-Type Mechanisms Modulate Allosteric Gating in Two-Pore-Domain Potassium Channel TREK-2.

Authors:  Ren-Gong Zhuo; Peng Peng; Xiao-Yan Liu; Hai-Tao Yan; Jiang-Ping Xu; Jian-Quan Zheng; Xiao-Li Wei; Xiao-Yun Ma
Journal:  Front Cell Neurosci       Date:  2016-05-13       Impact factor: 5.505

10.  Inactivation gating of Kv7.1 channels does not involve concerted cooperative subunit interactions.

Authors:  Eshcar Meisel; William Tobelaim; Meidan Dvir; Yoni Haitin; Asher Peretz; Bernard Attali
Journal:  Channels (Austin)       Date:  2018-01-01       Impact factor: 2.581

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