Restricted collision coupling of the adenosine A2Areceptor is due to its agonist-induced confinement in the membrane
© Thurner et al; licensee BioMed Central Ltd. 2012
Published: 17 September 2012
The A2A adenosine receptor is of interest because of several reasons. (i) It is a frequently blocked pharmacological target, because it is the site of action of caffeine. (ii) It has a long C-terminus that provides a docking site for several proteins, which direct the fate of the receptor from its synthesis to its lysosomal degradation. (iii) The A2A receptor can only promote activation of a limited number of available Gs molecules. This coupling mode was termed restricted collision coupling. (iv) Most G protein-coupled receptors carry one or several cysteine residues in their C-terminus which is subject to palmitoylation to anchor and stabilize the amphipathic helix 8; the A2A receptor lacks this palmitoylation site. We explored the hypothesis that there is a causal link between the absence of a palmitoyl moiety and restricted collision coupling.
We constructed a mutant A2A receptor, R309C, which underwent palmitoylation as verified by both mass spectrometry and metabolic labeling. Radioligand binding, cAMP accumulation and Western blotting were performed to determine its signaling properties. Using single particle tracking of quantum dot-labeled receptors we compared diffusivity and diffusion mode of wild-type and mutant A2A receptors.
In contrast to the wild-type receptor, the concentration-response curve for agonist-induced cAMP accumulation was shifted to the left with increasing expression levels of A2A receptor R309C. Single particle tracking demonstrated that agonist activation resulted in a decline in mean square displacement of both receptors, but the drop was substantially more pronounced for the wild-type receptor. In addition, in the agonist-bound state, the wild-type receptor was frequently subject to confinement events; these were rarely seen with the palmitoylated A2A receptor R309C.
Taken together, the observations link restricted collision coupling to diffusion limits imposed by the absence of a palmitoyl moiety in the C-terminus of the A2A receptor.
This work was supported by the Austrian Sciences Fund (FWF) and the Medical University of Vienna.
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