High-Resolution Crystal Structure of an Engineered Human β 2 -Adrenergic G Protein–Coupled Receptor
Scripps Research Institute · Stanford University
Abstract
Heterotrimeric guanine nucleotide-binding protein (G protein)-coupled receptors constitute the largest family of eukaryotic signal transduction proteins that communicate across the membrane. We report the crystal structure of a human beta2-adrenergic receptor-T4 lysozyme fusion protein bound to the partial inverse agonist carazolol at 2.4 angstrom resolution. The structure provides a high-resolution view of a human G protein-coupled receptor bound to a diffusible ligand. Ligand-binding site accessibility is enabled by the second extracellular loop, which is held out of the binding cavity by a pair of closely spaced disulfide bridges and a short helical segment within the loop. Cholesterol, a necessary…
Citation impact
- FWCI
- 121.62
- Percentile
- 100%
- References
- 69
Authors
11- VCVadim CherezovCorresponding
Scripps Research Institute, Stanford University
- DMDaniel M. RosenbaumCorresponding
Scripps Research Institute, Stanford University
- MAMichael A. Hanson
Scripps Research Institute, Stanford University
- SGSøren G. F. Rasmussen
Scripps Research Institute, Stanford University
- FSFoon Sun Thian
Scripps Research Institute, Stanford University
Topics & keywords
- Receptor
- Adrenergic receptor
- Resolution (logic)
- Chemistry
- Biophysics
- Cell biology
- Biology
- Biochemistry