Domains for activation and inactivation in G protein-coupled receptors - A mutational analysis of constitutive activity of the adenosine A sub(2B) receptor

• Published in: Biochemical pharmacology 2014-11, Vol.92 (2), p.348-357
• Main Authors: Peeters, Miriam C, Li, Qilan, Elands, Rachel, Westen, Gerard JPvan, Lenselink, Eelke B, Mueller, Christa E, IJzerman, Adriaan P
• Format: Article
• Language: English
• ISSN: 0006-2952
• DOI: 10.1016/j.bcp.2014.08.022

G protein-coupled receptors (GPCRs) are a major drug target and can be activated by a range of stimuli, from photons to proteins. Most, if not all, GPCRs also display a basal level of biological response in the absence of such a stimulus. This level of so-called constitutive activity results from a delicate energy equilibrium that exists between the active and the inactive state of the receptor and is the first determinant in the GPCR activation mechanism. Here we describe new insights in specific regions of the adenosine A sub(2B) receptor that are essential in activation and inactivation. We developed a new screening method using the MMY24 S. Cerevisiae strain by which we were able to screen for constitutively inactive mutants receptors (CIMs). We applied this screening method on a mutagenic library of the adenosine A sub(2B) receptor, where random mutations were introduced in transmembrane domains four and five (TM4 and TM5) linked by extracellular loop 2 (EL2). The screen resulted in the identification of 22 single and double mutant receptors, all showing a decrease in constitutive activity as well as in agonist potency. By comparing these results with a previous screen of the same mutagenic library for constitutively active mutant receptors (CAMs), we discovered specific regions in this G protein-coupled receptor involved in either inactivation or activation or both. The results suggest the activation mechanism of GPCRs to be much less restricted to sites of high conservation or direct interaction with the ligand or G protein and illustrate how dynamic the activation process of GPCRs is.