@article {Nie8758, author = {Jingjiang Nie and Deborah L. Lewis}, title = {Structural Domains of the CB1 Cannabinoid Receptor That Contribute to Constitutive Activity and G-Protein Sequestration}, volume = {21}, number = {22}, pages = {8758--8764}, year = {2001}, doi = {10.1523/JNEUROSCI.21-22-08758.2001}, publisher = {Society for Neuroscience}, abstract = {The CB1 cannabinoid receptor is a constitutively active receptor that can sequester Gi/o-proteins and prevent other Gi/o-coupled receptors from signaling (Bouaboula et al., 1997; Pan et al., 1998; Vasquez and Lewis, 1999). G-protein sequestration occurs because the population of CB1 cannabinoid receptors exists in both an inactive G-protein-precoupled RGGDP state and a constitutively active R*GGTPstate. We tested the hypothesis that the distal C-terminal tail acts to prevent G-protein activation. We found that truncation of the distal C-terminal tail of the CB1 receptor (CB1{\textendash}417) enhanced both the constitutive activity and the ability of the receptor to sequester G-proteins. In addition, we tested the hypothesis that the conserved aspartate (D2.50) in the second transmembrane domain of the CB1 cannabinoid receptor is crucial for constitutive activity and G-protein sequestration. We found that the mutation of aspartate to asparagine (CB1-D164N) abolished G-protein sequestration and constitutive receptor activity without disrupting agonist-stimulated activity. We conclude that the CB1-D164N mutation and the C-terminal truncation shift the population of receptors in opposite directions. The CB1-D164N mutation shifts the receptor into an inactive R state upcoupled from G-proteins, whereas the C-terminal truncation (CB1{\textendash}417) shifts the receptor into the active R*GGTP state. Thus the distal C-terminal tail acts to constrain the receptor from activating G-proteins, whereas the aspartate (D2.50) in the second transmembrane domain stabilizes the receptor in both the inactive RGGDP state and the active R*GGTP state.}, issn = {0270-6474}, URL = {https://www.jneurosci.org/content/21/22/8758}, eprint = {https://www.jneurosci.org/content/21/22/8758.full.pdf}, journal = {Journal of Neuroscience} }