Subunit-dependent assembly of inward-rectifier K+ channels

Proc Biol Sci. 1995 Aug 22;261(1361):251-61. doi: 10.1098/rspb.1995.0145.

Abstract

Inward-rectifier, G-protein-regulated and ATP-dependent K+ channels form a novel gene family of related proteins which share two transmembrane segments as a common structural feature. These K+ channels are only distantly related to the voltage-gated Shaker-type K+ channels comprising six transmembrane segments. Although the quaternary structure of voltage-gated K+ channels has been extensively studied in the past, little is known about subunit assembly of inward-rectifier K+ channels. Differential sensitivity of inward-rectifier K+ channels to voltage-dependent pore block by spermine was used to analyse subunit assembly. It is shown that inward-rectifier K+ channel proteins are composed of four subunits whose assembly obeys the rules of a binomial distribution. 'Strong' and 'mild' inward-rectifier K+ channel subunits (BIR10 and ROMK1) which are co-expressed in individual auditory hair cells form hetero-tetramers. Distribution of these hetero-tetramers, however, is not binomial. Hetero- and homo-oligomeric channels form with similar probabilities resulting in independent channel populations with distinct functional properties.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adenosine Triphosphate / metabolism
  • Animals
  • Base Sequence
  • Cloning, Molecular
  • DNA Primers / genetics
  • Female
  • GTP-Binding Proteins / metabolism
  • Gene Expression
  • Hair Cells, Auditory, Outer / metabolism
  • Kinetics
  • Molecular Sequence Data
  • Oocytes / metabolism
  • Polymerase Chain Reaction
  • Potassium Channels / chemistry*
  • Potassium Channels / genetics
  • Potassium Channels / metabolism
  • Protein Conformation
  • Rats
  • Recombinant Proteins / chemistry
  • Recombinant Proteins / genetics
  • Recombinant Proteins / metabolism
  • Xenopus

Substances

  • DNA Primers
  • Potassium Channels
  • Recombinant Proteins
  • Adenosine Triphosphate
  • GTP-Binding Proteins