Structure and different conformational states of native AMPA receptor complexes

Nature. 2005 Feb 3;433(7025):545-9. doi: 10.1038/nature03328.


Ionotropic glutamate receptors mediate fast excitatory synaptic transmission in the central nervous system. Their modulation is believed to affect learning and memory, and their dysfunction has been implicated in the pathogenesis of neurological and psychiatric diseases. Despite a wealth of functional data, little is known about the intact, three-dimensional structure of these ligand-gated ion channels. Here, we present the structure of native AMPA receptors (alpha-amino-3-hydroxy-5-methyl-4-isoxazole propionic acid; AMPA-Rs) purified from rat brain, as determined by single-particle electron microscopy. Unlike the homotetrameric recombinant GluR2 (ref. 3), the native heterotetrameric AMPA-R adopted various conformations, which reflect primarily a variable separation of the two dimeric extracellular amino-terminal domains. Members of the stargazin/TARP family of transmembrane proteins co-purified with AMPA-Rs and contributed to the density representing the transmembrane region of the complex. Glutamate and cyclothiazide markedly altered the conformational equilibrium of the channel complex, suggesting that desensitization is related to separation of the N-terminal domains. These data provide a glimpse of the conformational changes of an important ligand-gated ion channel of the brain.

Publication types

  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Animals
  • Benzothiadiazines / pharmacology
  • Brain
  • Cell Membrane / chemistry
  • Cell Membrane / metabolism
  • Glutamic Acid / metabolism
  • Glutamic Acid / pharmacology
  • Ligands
  • Models, Molecular
  • Multiprotein Complexes / chemistry
  • Multiprotein Complexes / metabolism
  • Multiprotein Complexes / ultrastructure
  • Protein Structure, Quaternary / drug effects
  • Protein Structure, Tertiary / drug effects
  • Rats
  • Receptors, AMPA / chemistry
  • Receptors, AMPA / metabolism*
  • Receptors, AMPA / ultrastructure*


  • Benzothiadiazines
  • Ligands
  • Multiprotein Complexes
  • Receptors, AMPA
  • Glutamic Acid
  • cyclothiazide