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Biochim Biophys Acta Biomembr. 2019 Apr 1;1861(4):760-767. doi: 10.1016/j.bbamem.2019.01.001. Epub 2019 Jan 8.

Membrane cholesterol depletion reduces downstream signaling activity of the adenosine A2A receptor.

Author information

1
Department of Chemical and Biomolecular Engineering, Tulane University, New Orleans, LA, United States.
2
Department of Physics and Astronomy, University of Delaware, Newark, DE, United States.
3
Department of Integrative Biology and Pharmacology, University of Texas- Houston, Houston, TX, United States.
4
Department of Chemical and Biomolecular Engineering, Tulane University, New Orleans, LA, United States. Electronic address: anne.robinson@cmu.edu.

Abstract

Cholesterol has been shown to modulate the activity of multiple G Protein-coupled receptors (GPCRs), yet whether cholesterol acts through specific interactions, indirectly via modifications to the membrane, or via both mechanisms is not well understood. High-resolution crystal structures of GPCRs have identified bound cholesterols; based on a β2-adrenergic receptor (β2AR) structure bound to cholesterol and the presence of conserved amino acids in class A receptors, the cholesterol consensus motif (CCM) was identified. Here in mammalian cells expressing the adenosine A2A receptor (A2AR), ligand dependent production of cAMP is reduced following membrane cholesterol depletion with methyl-beta-cyclodextrin (MβCD), indicating that A2AR signaling is dependent on cholesterol. In contrast, ligand binding is not dependent on cholesterol depletion. All-atom molecular simulations suggest that cholesterol interacts specifically with the CCM when the receptor is in an active state, but not when in an inactive state. Taken together, the data support a model of receptor state-dependent binding between cholesterol and the CCM, which could facilitate both G-protein coupling and downstream signaling of A2AR.

KEYWORDS:

Downstream signaling; G-protein coupled receptor; Ligand binding; Membrane protein; Simulation

PMID:
30629951
PMCID:
PMC6383678
[Available on 2020-04-01]
DOI:
10.1016/j.bbamem.2019.01.001

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