The S1 helix critically regulates the finely tuned gating of Kv11.1 channels

J Biol Chem. 2017 May 5;292(18):7688-7705. doi: 10.1074/jbc.M117.779298. Epub 2017 Mar 9.

Abstract

Congenital mutations in the cardiac Kv11.1 channel can cause long QT syndrome type 2 (LQTS2), a heart rhythm disorder associated with sudden cardiac death. Mutations act either by reducing protein expression at the membrane and/or by perturbing the intricate gating properties of Kv11.1 channels. A number of clinical LQTS2-associated mutations have been reported in the first transmembrane segment (S1) of Kv11.1 channels, but the role of this region of the channel is largely unexplored. In part, this is due to problems defining the extent of the S1 helix, as a consequence of its low sequence homology with other Kv family members. Here, we used NMR spectroscopy and electrophysiological characterization to show that the S1 of Kv11.1 channels extends seven helical turns, from Pro-405 to Phe-431, and is flanked by unstructured loops. Functional analysis suggests that pre-S1 loop residues His-402 and Tyr-403 play an important role in regulating the kinetics and voltage dependence of channel activation and deactivation. Multiple residues within the S1 helix also play an important role in fine-tuning the voltage dependence of activation, regulating slow deactivation, and modulating C-type inactivation of Kv11.1 channels. Analyses of LQTS2-associated mutations in the pre-S1 loop or S1 helix of Kv11.1 channels demonstrate perturbations to both protein expression and most gating transitions. Thus, S1 region mutations would reduce both the action potential repolarizing current passed by Kv11.1 channels in cardiac myocytes, as well as the current passed in response to premature depolarizations that normally helps protect against the formation of ectopic beats.

Keywords: biophysics; cardiovascular disease; channel activation; electrophysiology; hERG; ion channel; mutagenesis in vitro; nuclear magnetic resonance (NMR); oocyte; potassium channel.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Animals
  • ERG1 Potassium Channel / genetics
  • ERG1 Potassium Channel / metabolism*
  • Humans
  • Ion Channel Gating / physiology*
  • Long QT Syndrome / genetics
  • Long QT Syndrome / metabolism
  • Mutation, Missense
  • Myocytes, Cardiac / metabolism*
  • Protein Structure, Secondary
  • Xenopus laevis

Substances

  • ERG1 Potassium Channel
  • KCNH2 protein, human

Associated data

  • PDB/5K7L