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9CBL

Cryo-EM structure of epinephrine-bound alpha-2A-adrenergic receptor in complex with heterotrimeric Gi-protein

Summary for 9CBL
Entry DOI10.2210/pdb9cbl/pdb
EMDB information45425
DescriptorGuanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, Guanine nucleotide-binding protein G(I)/G(S)/G(O) subunit gamma-2, ... (5 entities in total)
Functional Keywordsgpcr, adrenergic receptor, signaling protein
Biological sourceRattus norvegicus (Norway rat)
More
Total number of polymer chains4
Total formula weight143176.96
Authors
Lou, J.S.,Su, M.,Wang, J.,Do, H.N.,Miao, Y.,Huang, X.Y. (deposition date: 2024-06-19, release date: 2024-09-11, Last modification date: 2024-10-16)
Primary citationLou, J.S.,Su, M.,Wang, J.,Do, H.N.,Miao, Y.,Huang, X.Y.
Distinct binding conformations of epinephrine with alpha- and beta-adrenergic receptors.
Exp.Mol.Med., 56:1952-1966, 2024
Cited by
PubMed Abstract: Agonists targeting α-adrenergic receptors (ARs) are used to treat diverse conditions, including hypertension, attention-deficit/hyperactivity disorder, pain, panic disorders, opioid and alcohol withdrawal symptoms, and cigarette cravings. These receptors transduce signals through heterotrimeric Gi proteins. Here, we elucidated cryo-EM structures that depict α-AR in complex with Gi proteins, along with the endogenous agonist epinephrine or the synthetic agonist dexmedetomidine. Molecular dynamics simulations and functional studies reinforce the results of the structural revelations. Our investigation revealed that epinephrine exhibits different conformations when engaging with α-ARs and β-ARs. Furthermore, α-AR and β-AR (primarily coupled to Gs, with secondary associations to Gi) were compared and found to exhibit different interactions with Gi proteins. Notably, the stability of the epinephrine-α-AR-Gi complex is greater than that of the dexmedetomidine-α-AR-Gi complex. These findings substantiate and improve our knowledge on the intricate signaling mechanisms orchestrated by ARs and concurrently shed light on the regulation of α-ARs and β-ARs by epinephrine.
PubMed: 39218975
DOI: 10.1038/s12276-024-01296-x
PDB entries with the same primary citation
Experimental method
ELECTRON MICROSCOPY (2.8 Å)
Structure validation

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PDB entries from 2024-11-13

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