Received for publication May 29, 2007.
Revised October 15, 2007.
Accepted for publication October 16, 2007.

CONSTITUTIVELY ACTIVE MUTANTS OF THE HISTAMINE H₁ RECEPTOR SUGGEST A CONSERVED HYDROPHOBIC ASPARAGINE-CAGE THAT CONSTRAINS THE ACTIVATION OF CLASS A GPCRS

Abstract

The aim of this study was to create and characterize constitutively-active mutant (CAM) histamine H₁ receptors (H₁R) using random mutagenesis methodology to further investigate the activation process of the rhodopsin-like family of G protein-coupled receptors (GPCRs). This approach identified position 6.40 in TM 6 as a "hot spot" since mutation of Ile6.40⁴²⁰ either to Glu, Gly, Ala, Arg, Lys, or Ser results in highly active CAM H₁Rs, for which almost no histamine-induced receptor activation response can be detected. The highly conserved hydrophobic amino acid at position 6.40 defines, in a computational model of the H₁R, the asparagine cage motif that restrains the side chain of Asn7.49 of the NPxxY motif towards TM 6 in the inactive state of the receptor. Mutation of the asparagine cage into Ala or Gly, removing the interfering bulky constraints, increases the constitutive activity of the receptor. The fact that the Ile6.40⁴²⁰Arg/Lys/Glu mutant receptors are highly active CAM H₁Rs leads us to suggest that a positively charged residue, presumably the highly conserved Arg3.50 from the DRY motif, interacts in a direct or an indirect (through other side chains or/and internal water molecules) manner with the acidic Asp2.50··Asn7.49 pair for receptor activation.

Key words: Histamine, Gq/11 family, Structure-activity relationships and modeling, Mutagenesis/Chimeric approaches, Receptor binding studies