Cannabis elicits its mood-enhancing and analgesic effects through the cannabinoid receptor 1 (CB1), a G protein-coupled receptor (GPCR) that signals primarily through the adenylyl cyclase-inhibiting heterotrimeric G protein Gi. Activation of CB1-Gi signaling pathways holds potential for treating a number of neurological disorders and is thus crucial to understand the mechanism of Gi activation by CB1. Here, we present the structure of the CB1-Gi signaling complex bound to the highly potent agonist MDMB-Fubinaca (FUB), a recently emerged illicit synthetic cannabinoid infused in street drugs that have been associated with numerous overdoses and fatalities. The structure illustrates how FUB stabilizes the receptor in an active state to facilitate nucleotide exchange in Gi. The results compose the structural framework to explain CB1 activation by different classes of ligands and provide insights into the G protein coupling and selectivity mechanisms adopted by the receptor.
Journal article
Structure of a Signaling Cannabinoid Receptor 1-G Protein Complex
Cell, Vol.176(3), pp.448-458.e12
24/Jan/2019
PMID: 30639101
Abstract
Details
- Title
- Structure of a Signaling Cannabinoid Receptor 1-G Protein Complex
- Creators
- Kaavya Krishna Kumar (null) - Stanford UniversityMoran Shalev-Benami (null) - 972WIS_INST___9Michael J. Robertson (null) - Stanford UniversityHongli Hu (null) - Stanford UniversitySamuel D. Banister (null) - Stanford UniversityScott A. Hollingsworth (null) - Stanford UniversityNaomi R. Latorraca (null) - Stanford UniversityHideaki E. Kato (null) - Stanford UniversityDaniel Hilger (null) - Stanford UniversityShoji Maeda (null) - Stanford UniversityWilliam I. Weis (null) - Stanford UniversityDavid L. Farrens (null) - Oregon Health & Science UniversityRon O. Dror (null) - Stanford UniversitySanjay V. Malhotra (null) - Stanford UniversityBrian K. Kobilka (Corresponding Author) - Stanford UniversityGeorgios Skiniotis (null) - Stanford University
- Resource Type
- Journal article
- Publication Details
- Cell, Vol.176(3), pp.448-458.e12; 24/Jan/2019
- Number of pages
- 23
- Language
- English
- DOI
- https://doi.org/10.1016/j.cell.2018.11.040
- PMID
- 30639101
- Grant note
- K.K. was supported by the NHMRC, Australia CJ Martin Fellowship. The work is supported by the NIH (R37DA036246 to B.K.K. and G.S. and R01GM083118 to B.K.K.). B.K.K. is a Chan Zuckerberg Biohub investigator.
- Record Identifier
- 993267044503596
Metrics
8 Record Views