RT Journal Article SR Electronic T1 Internal Trafficking and Surface Mobility of a Functionally Intact β2-Adrenergic Receptor-Green Fluorescent Protein Conjugate JF Molecular Pharmacology JO Mol Pharmacol FD American Society for Pharmacology and Experimental Therapeutics SP 177 OP 184 DO 10.1124/mol.51.2.177 VO 51 IS 2 A1 Larry S. Barak A1 Stephen S. G. Ferguson A1 Jie Zhang A1 Christopher Martenson A1 Tobias Meyer A1 Marc G. Caron YR 1997 UL http://molpharm.aspetjournals.org/content/51/2/177.abstract AB The β2-adrenergic receptor (β2AR) is prototypic of the large family of G protein-coupled receptors (GPCRs) whose desensitization and resensitization are regulated by intracellular kinases, arrestin proteins, phosphatases, and ill-defined components of the cellular endocytic machinery. The study of β2AR signal transduction and behavior in living cells is technically difficult because of the relatively low cellular expression of the receptor and a lack of useful biological reagents. Availability of a functional β2AR tagged with the highly sensitive Green Fluorescent Protein (GFP) could allow measurements of the various properties of the β2AR. We demonstrate that a fully functional β2AR/GFP can be engineered. In mammalian cells, β2AR/S65T/GFP demonstrates strong, diffuse plasma membrane fluorescence when observed with 480 nm excitation. The fluorescent receptor binds agonist and antagonist, stimulates adenylyl cyclase, undergoes phosphorylation, and is internalized in a manner indistinguishable from wild-type receptor. We then show that its internal trafficking and surface mobility can be determined by measuring only the endogenous fluorescence of the conjugate. β2AR/S65T/GFP was found to be localized on endosomal membranes in living cells within minutes of agonist treatment, and within 15 min it is observed in more complicated structures formed from fusion of multiple endosomes. Finally, its free diffusion (diffusion coefficient, 4.0–12 × 10−9 cm2/sec) was assessed on living cells using photobleaching recovery measurements. This approach and the fidelity of the biochemical properties of the β2AR/S65T/GFP demonstrate that real-time optical measurements of β2AR (as well as other GPCR) interactions and dynamics on living cells are feasible.