Ligand-Directed Labeling of the Adenosine A<sub>1</sub> Receptor in Living Cells
Eleonora Comeo, Joëlle Goulding, Chia-Yang Lin, Marleen Groenen, Jeanette Woolard, Nicholas D. Kindon, Clare R. Harwood, Simon Platt, Stephen J. Briddon, Laura E. Kilpatrick, Peter J. Scammells, Stephen J. Hill, Barrie Kellam
Abstract
High Resolution Image Download MS PowerPoint Slide The study of protein function and dynamics in their native cellular environment is essential for progressing fundamental science. To overcome the requirement of genetic modification of the protein or the limitations of dissociable fluorescent ligands, ligand-directed (LD) chemistry has most recently emerged as a complementary, bioorthogonal approach for labeling native proteins. Here, we describe the rational design, development, and application of the first ligand-directed chemistry approach for labeling the A 1 AR in living cells. We pharmacologically demonstrate covalent labeling of A 1 AR expressed in living cells while the orthosteric binding site remains available. The probes were imaged using confocal microscopy and fluorescence correlation spectroscopy to study A 1 AR localization and dynamics in living cells. Additionally, the probes allowed visualization of the specific localization of A 1 ARs endogenously expressed in dorsal root ganglion (DRG) neurons. LD probes developed here hold promise for illuminating ligand-binding, receptor signaling, and trafficking of the A 1 AR in more physiologically relevant environments.