Structure of an Agonist-Bound Human A 2A Adenosine Receptor
Scripps Research Institute · San Diego Supercomputer Center · +2 more institutions
Abstract
Activation of G protein-coupled receptors upon agonist binding is a critical step in the signaling cascade for this family of cell surface proteins. We report the crystal structure of the A(2A) adenosine receptor (A(2A)AR) bound to an agonist UK-432097 at 2.7 angstrom resolution. Relative to inactive, antagonist-bound A(2A)AR, the agonist-bound structure displays an outward tilt and rotation of the cytoplasmic half of helix VI, a movement of helix V, and an axial shift of helix III, resembling the changes associated with the active-state opsin structure. Additionally, a seesaw movement of helix VII and a shift of extracellular loop 3 are likely specific to A(2A)AR and its ligand. The results define the…
Citation impact
- FWCI
- 50.55
- Percentile
- 100%
- References
- 37
Authors
8Topics & keywords
- Agonist
- Chemistry
- Helix (gastropod)
- Receptor
- Ligand (biochemistry)
- G protein-coupled receptor
- Stereochemistry
- Biophysics