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Structural implications of hERG K+ channel block by a high affinity minimally-structured blocker

Research output: Contribution to journalArticle

Original languageEnglish
Pages (from-to)7040-7057
Number of pages38
JournalJournal of Biological Chemistry
Volume293
Issue number18
Early online date15 Mar 2018
DOIs
DateAccepted/In press - 15 Mar 2018
DateE-pub ahead of print - 15 Mar 2018
DatePublished (current) - 4 May 2018

Abstract

Cardiac potassium channels encoded byhuman Ether-à-go-go Related Gene (hERG)are major targets for structurally diverse drugs associated with acquired long QT syndrome. This study characterized hERG channel inhibition by a minimally structured high affinity hERG inhibitor, Cavalli-2, composed of three phenyl groups linked by polymethylene spacers around a central amino group, chosen to probe the spatial arrangement of side chain groups in the high-affinity drug binding site of the hERG pore. hERG current (IhERG) recorded at physiological temperature from HEK 293 cells was inhibited with an IC50of 35.6 nM, with time- and voltage-dependence characteristic of blockade contingent upon channel gating. Potency of Cavalli-2 action was markedly reduced for attenuated-inactivation mutants located near (S620T; 54-fold) and remote from (N588K; 15-fold) the channel pore. The S6 Y652A and F656A mutations decreased inhibitory potency 17- and 75-fold respectively, whilst T623A and S624A at the base of the selectivity filter also decreased potency (16- and 7-fold respectively). The S5 helix F557L mutation decreased potency 10-fold and both F557L and Y652A mutations eliminated voltage dependence of inhibition. Computational docking using the recent cryo-EM structure of an open channel hERG construct could only partially recapitulate experimental data, and the high dependence of Cavalli-2 block on F656 is not readily explainable in that structure. A small clockwise rotation of the inner (S6) helix of the hERG pore from its configuration in the cryo-EM structure may be required to optimize F656 side chain orientations compatible with high affinity block.

    Research areas

  • hERG, K+ channel, Long QT syndrome, Alanine scan mutagenesis, Computational docking

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    Rights statement: This is the final published version of the article (version of record). It first appeared online via ASBMB at http://www.jbc.org/content/293/18/7040 . Please refer to any applicable terms of use of the publisher.

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