Allosteric Activation Mechanism of the Alpha 1 Beta 2 Gamma 2 Gamma-Aminobutyric Acid Type A Receptor Revealed by Mutation of the Conserved M2 Leucine

Biophys J. 1999 Nov;77(5):2542-51. doi: 10.1016/s0006-3495(99)77089-x.

Abstract

A conserved leucine residue in the midpoint of the second transmembrane domain (M2) of the ligand-activated ion channel family has been proposed to play an important role in receptor activation. In this study, we assessed the importance of this leucine in the activation of rat alpha 1 beta 2 gamma 2 GABA receptors expressed in Xenopus laevis oocytes by site-directed mutagenesis and two-electrode voltage clamp. The hydrophobic conserved M2 leucines in alpha1(L263), beta2(L259), and gamma 2(L274) subunits were mutated to the hydrophilic amino acid residue serine and coexpressed in all possible combinations with their wild-type and/or mutant counterparts. The mutation in any one subunit decreased the EC(50) and created spontaneous openings that were blocked by picrotoxin and, surprisingly, by the competitive antagonist bicuculline. The magnitudes of the shifts in GABA EC(50) and picrotoxin IC(50) as well as the degree of spontaneous openings were all correlated with the number of subunits carrying the leucine mutation. Simultaneous mutation of the GABA binding site (beta 2Y157S; increased the EC(50)) and the conserved M2 leucine (beta 2L259S; decreased the EC(50)) produced receptors with the predicted intermediate agonist sensitivity, indicating the two mutations affect binding and gating independently. The results are discussed in light of a proposed allosteric activation mechanism.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Allosteric Regulation / drug effects
  • Animals
  • Bicuculline / pharmacology
  • Conserved Sequence*
  • Dose-Response Relationship, Drug
  • Electric Conductivity
  • Female
  • GABA-A Receptor Antagonists / pharmacology
  • Hydrophobic and Hydrophilic Interactions
  • Ion Channel Gating / drug effects
  • Leucine*
  • Mutagenesis, Site-Directed
  • Mutation*
  • Picrotoxin / pharmacology
  • Protein Structure, Tertiary
  • Rats
  • Receptors, GABA-A / chemistry*
  • Receptors, GABA-A / genetics
  • Receptors, GABA-A / metabolism*
  • gamma-Aminobutyric Acid / pharmacology

Substances

  • GABA-A Receptor Antagonists
  • Gabra1 protein, rat
  • Gabrb2 protein, rat
  • Gabrg2 protein, rat
  • Receptors, GABA-A
  • Picrotoxin
  • gamma-Aminobutyric Acid
  • Leucine
  • Bicuculline