Pharmacology of voltage-gated and calcium-activated potassium channels

Curr Opin Chem Biol. 1999 Aug;3(4):448-58. doi: 10.1016/S1367-5931(99)80066-0.

Abstract

Several important new findings have furthered the development of voltage-gated and calcium-activated potassium channel pharmacology. The molecular constituents of several members of these large ion channel families were identified. Small-molecule modulators of some of these channels were reported, including correolide, the first potent, small-molecule, natural product inhibitor of the Shaker family of voltage-gated potassium channels to be disclosed. The initial crystal structure of a bacterial potassium channel was determined; this work gives a physical basis for understanding the mechanisms of ion selectivity and ion conduction. With the recent molecular characterization of a potassium channel structure and the discovery of new templates for channel modulatory agents, the ability to rationally identify and develop potassium channel agonists and antagonists may become a reality in the near future.

Publication types

  • Review

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Calcium / pharmacology*
  • Carbohydrate Sequence
  • Ion Channel Gating*
  • Molecular Sequence Data
  • Potassium Channel Blockers
  • Potassium Channels / agonists*
  • Potassium Channels / physiology
  • Sequence Homology, Amino Acid
  • Toxins, Biological / chemistry
  • Toxins, Biological / pharmacology

Substances

  • Potassium Channel Blockers
  • Potassium Channels
  • Toxins, Biological
  • Calcium