Control of KirBac3.1 potassium channel gating at the interface between cytoplasmic domains

J Biol Chem. 2014 Jan 3;289(1):143-51. doi: 10.1074/jbc.M113.501833. Epub 2013 Nov 20.

Abstract

KirBac channels are prokaryotic homologs of mammalian inwardly rectifying potassium (Kir) channels, and recent structures of KirBac3.1 have provided important insights into the structural basis of gating in Kir channels. In this study, we demonstrate that KirBac3.1 channel activity is strongly pH-dependent, and we used x-ray crystallography to determine the structural changes that arise from an activatory mutation (S205L) located in the cytoplasmic domain (CTD). This mutation stabilizes a novel energetically favorable open conformation in which changes at the intersubunit interface in the CTD also alter the electrostatic potential of the inner cytoplasmic cavity. These results provide a structural explanation for the activatory effect of this mutation and provide a greater insight into the role of the CTD in Kir channel gating.

Keywords: Channel Gating; Crystal Structure; Ion Channels; Kir Channel; KirBac; Membrane Proteins; Molecular Dynamics; Potassium Channels.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Bacterial Proteins / chemistry*
  • Bacterial Proteins / genetics
  • Bacterial Proteins / metabolism
  • Ion Channel Gating / physiology
  • Magnetospirillum / chemistry*
  • Magnetospirillum / genetics
  • Magnetospirillum / metabolism
  • Mutation, Missense
  • Potassium Channels, Inwardly Rectifying / chemistry*
  • Potassium Channels, Inwardly Rectifying / genetics
  • Potassium Channels, Inwardly Rectifying / metabolism
  • Protein Structure, Tertiary

Substances

  • Bacterial Proteins
  • Potassium Channels, Inwardly Rectifying

Associated data

  • PDB/4LP8