Inverse coupling in leak and voltage-activated K+ channel gates underlies distinct roles in electrical signaling

Nat Struct Mol Biol. 2009 Jan;16(1):71-9. doi: 10.1038/nsmb.1525. Epub 2008 Dec 21.

Abstract

Voltage-activated (Kv) and leak (K(2P)) K(+) channels have key, yet distinct, roles in electrical signaling in the nervous system. Here we examine how differences in the operation of the activation and slow inactivation pore gates of Kv and K(2P) channels underlie their unique roles in electrical signaling. We report that (i) leak K(+) channels possess a lower activation gate, (ii) the activation gate is an important determinant controlling the conformational stability of the K(+) channel pore, (iii) the lower activation and upper slow inactivation gates of leak channels cross-talk and (iv) unlike Kv channels, where the two gates are negatively coupled, these two gates are positively coupled in K(2P) channels. Our results demonstrate how basic thermodynamic properties of the K(+) channel pore, particularly conformational stability and coupling between gates, underlie the specialized roles of Kv and K(2P) channel families in electrical signaling.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Conserved Sequence
  • Drosophila Proteins / chemistry
  • Drosophila Proteins / physiology
  • Drug Stability
  • Electrophysiology
  • Ion Channel Gating / physiology*
  • Models, Molecular
  • Molecular Sequence Data
  • Potassium Channels, Tandem Pore Domain / chemistry
  • Potassium Channels, Tandem Pore Domain / physiology*
  • Potassium Channels, Voltage-Gated / antagonists & inhibitors
  • Potassium Channels, Voltage-Gated / chemistry
  • Potassium Channels, Voltage-Gated / physiology*
  • Potentiometry
  • Protein Conformation
  • Sequence Alignment
  • Signal Transduction

Substances

  • Drosophila Proteins
  • Potassium Channels, Tandem Pore Domain
  • Potassium Channels, Voltage-Gated