High-conductance calcium-activated potassium channels; structure, pharmacology, and function

J Bioenerg Biomembr. 1996 Jun;28(3):255-67. doi: 10.1007/BF02110699.

Abstract

High-conductance calcium-activated potassium (maxi-K) channels comprise a specialized family of K+ channels. They are unique in their dual requirement for depolarization and Ca2+ binding for transition to the open, or conducting, state. Ion conduction through maxi-K channels is blocked by a family of venom-derived peptides, such as charybdotoxin and iberiotoxin. These peptides have been used to study function and structure of maxi-K channels, to identify novel channel modulators, and to follow the purification of functional maxi-K channels from smooth muscle. The channel consists of two dissimilar subunits, alpha and beta. The alpha subunit is a member of the slo Ca(2+)-activated K+ channel gene family and forms the ion conduction pore. The beta subunit is a structurally unique, membrane-spanning protein that contributes to channel gating and pharmacology. Potent, selective maxi-K channel effectors (both agonists and blockers) of low molecular weight have been identified from natural product sources. These agents, together with peptidyl inhibitors and site-directed antibodies raised against alpha and beta subunit sequences, can be used to anatomically map maxi-K channel expression, and to study the physiologic role of maxi-K channels in various tissues. One goal of such investigations is to determine whether maxi-K channels represent novel therapeutic targets.

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Charybdotoxin / metabolism
  • Diterpenes / metabolism
  • Glycosylation
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits
  • Large-Conductance Calcium-Activated Potassium Channel beta Subunits
  • Large-Conductance Calcium-Activated Potassium Channels
  • Models, Molecular
  • Molecular Sequence Data
  • Muscle, Smooth / metabolism
  • Peptides / metabolism
  • Potassium Channels / chemistry
  • Potassium Channels / pharmacology
  • Potassium Channels / physiology*
  • Potassium Channels, Calcium-Activated*
  • Protein Conformation
  • Scorpion Venoms / metabolism
  • Synapses / metabolism
  • Triterpenes / metabolism

Substances

  • Diterpenes
  • Large-Conductance Calcium-Activated Potassium Channel alpha Subunits
  • Large-Conductance Calcium-Activated Potassium Channel beta Subunits
  • Large-Conductance Calcium-Activated Potassium Channels
  • Peptides
  • Potassium Channels
  • Potassium Channels, Calcium-Activated
  • Scorpion Venoms
  • Triterpenes
  • maxikdiol
  • Charybdotoxin
  • iberiotoxin