Determining the correct stoichiometry of Kv2.1/Kv6.4 heterotetramers, functional in multiple stoichiometrical configurations

Proc Natl Acad Sci U S A. 2020 Apr 28;117(17):9365-9376. doi: 10.1073/pnas.1916166117. Epub 2020 Apr 13.

Abstract

The electrically silent (KvS) members of the voltage-gated potassium (Kv) subfamilies Kv5, Kv6, Kv8, and Kv9 selectively modulate Kv2 subunits by forming heterotetrameric Kv2/KvS channels. Based on the reported 3:1 stoichiometry of Kv2.1/Kv9.3 channels, we tested the hypothesis that Kv2.1/Kv6.4 channels express, in contrast to the assumed 3:1, in a 2:2 stoichiometry. We investigate the Kv2.1/Kv6.4 stoichiometry using single subunit counting and functional characterization of tetrameric concatemers. For selecting the most probable stoichiometry, we introduce a model-selection method that is applicable for any multimeric complex by investigating the stoichiometry of Kv2.1/Kv6.4 channels. Weighted likelihood calculations bring rigor to a powerful technique. Using the weighted-likelihood model-selection method and analysis of electrophysiological data, we show that Kv2.1/Kv6.4 channels express, in contrast to the assumed 3:1, in a 2:2 stoichiometry. Within this stoichiometry, the Kv6.4 subunits have to be positioned alternating with Kv2.1 to express functional channels. The variability in Kv2/KvS assembly increases the diversity of heterotetrameric configurations and extends the regulatory possibilities of KvS by allowing the presence of more than one silent subunit.

Keywords: Kv channels; model selection; silent subunits; single subunit counting.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Animals
  • Antibodies
  • Cell Line
  • Fibroblasts
  • Gene Expression Regulation
  • HEK293 Cells
  • Humans
  • Membrane Potentials
  • Mice
  • Oocytes / metabolism
  • Photobleaching
  • Potassium / metabolism*
  • Potassium Channels, Voltage-Gated / genetics
  • Potassium Channels, Voltage-Gated / metabolism*
  • Receptor Protein-Tyrosine Kinases / genetics
  • Recombinant Proteins
  • Shab Potassium Channels / genetics
  • Shab Potassium Channels / immunology
  • Shab Potassium Channels / metabolism*
  • Xenopus

Substances

  • Antibodies
  • KCNB1 protein, human
  • KCNG4 protein, human
  • Kcnb1 protein, mouse
  • Potassium Channels, Voltage-Gated
  • Recombinant Proteins
  • Shab Potassium Channels
  • Ltk protein, mouse
  • Receptor Protein-Tyrosine Kinases
  • Potassium

Grants and funding