Argiotoxin in the closed AMPA receptor channel: experimental and modeling study

Biochemistry. 2011 Sep 27;50(38):8213-20. doi: 10.1021/bi200617v. Epub 2011 Aug 29.

Abstract

Binding of argiotoxin in the closed state of Ca(2+)-permeable AMPA receptor channels was studied using electrophysiological and molecular modeling approaches. Experimental study unambiguously revealed that argiotoxin is trapped in the closed AMPA receptor channels after agonist dissociation. Docking of the argiotoxin to the channel model based on recently published X-ray structure demonstrated that the drug can be effectively accommodated in the cavity of the closed channel only if the terminal moiety of the molecule penetrates in the narrow portion of the pore below the selectivity filter. Combining these results, we conclude that the selectivity filter of the AMPA receptor channels is not sterically occluded in the closed state.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Sequence
  • Animals
  • Binding Sites
  • Brain / metabolism
  • Electrophysiological Phenomena
  • Indoleacetic Acids
  • Interneurons / drug effects
  • Interneurons / metabolism
  • Models, Molecular
  • Molecular Sequence Data
  • Phenylacetates / chemistry*
  • Phenylacetates / metabolism*
  • Phenylacetates / pharmacology
  • Polyamines / chemistry*
  • Polyamines / metabolism*
  • Polyamines / pharmacology
  • Protein Conformation
  • Rats
  • Rats, Wistar
  • Receptors, AMPA / antagonists & inhibitors
  • Receptors, AMPA / chemistry*
  • Receptors, AMPA / genetics
  • Receptors, AMPA / metabolism*
  • Spider Venoms / chemistry
  • Spider Venoms / metabolism
  • Spider Venoms / pharmacology
  • Thermodynamics

Substances

  • Indoleacetic Acids
  • Phenylacetates
  • Polyamines
  • Receptors, AMPA
  • Spider Venoms
  • argiotoxin-636