TY - JOUR T1 - Mutation of a Highly Conserved Aspartic Acid in the β<sub>2</sub> Adrenergic Receptor: Constitutive Activation, Structural Instability, and Conformational Rearrangement of Transmembrane Segment 6 JF - Molecular Pharmacology JO - Mol Pharmacol SP - 175 LP - 184 DO - 10.1124/mol.56.1.175 VL - 56 IS - 1 AU - Søren G.F. Rasmussen AU - Anne D. Jensen AU - George Liapakis AU - Pejman Ghanouni AU - Jonathan A. Javitch AU - Ulrik Gether Y1 - 1999/07/01 UR - http://molpharm.aspetjournals.org/content/56/1/175.abstract N2 - Movements of transmembrane segments (TMs) 3 and 6 play a key role in activation of G protein-coupled receptors. However, the underlying molecular processes that govern these movements, and accordingly control receptor activation, remain unclear. To elucidate the importance of the conserved aspartic acid (Asp-130) in the Asp-Arg-Tyr motif of the β2 adrenergic receptor (β2AR), we mutated this residue to asparagine (D130N) to mimic its protonated state, and to alanine (D130A) to fully remove the functionality of the side chain. Both mutants displayed evidence of constitutive receptor activation. In COS-7 cells expressing either D130N or D130A, basal levels of cAMP accumulation were clearly elevated compared with cells expressing the wild-type β2AR. Incubation of COS-7 cell membranes or purified receptor at 37°C revealed also a marked structural instability of both mutant receptors, suggesting that stabilizing intramolecular constraints had been disrupted. Moreover, we obtained evidence for a conformational rearrangement by mutation of Asp-130. In D130N, a cysteine in TM 6, Cys-285, which is not accessible in the wild-type β2AR, became accessible to methanethiosulfonate ethylammonium, a charged, sulfhydryl-reactive reagent. This is consistent with a counterclockwise rotation or tilting of TM 6 and provides for the first time structural evidence linking charge-neutralizing mutations of the aspartic acid in the DRY motif to the overall conformational state of the receptor. We propose that protonation of the aspartic acid leads to release of constraining intramolecular interactions, resulting in movements of TM 6 and, thus, conversion of the receptor to the active state. ER -