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-Structure paper
タイトル | Structures of β-adrenergic receptor in complex with Gs and ligands of different efficacies. |
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ジャーナル・号・ページ | Nat Commun, Vol. 13, Issue 1, Page 4095, Year 2022 |
掲載日 | 2022年7月14日 |
著者 | Minfei Su / Navid Paknejad / Lan Zhu / Jinan Wang / Hung Nguyen Do / Yinglong Miao / Wei Liu / Richard K Hite / Xin-Yun Huang / |
PubMed 要旨 | G-protein-coupled receptors (GPCRs) receive signals from ligands with different efficacies, and transduce to heterotrimeric G-proteins to generate different degrees of physiological responses. ...G-protein-coupled receptors (GPCRs) receive signals from ligands with different efficacies, and transduce to heterotrimeric G-proteins to generate different degrees of physiological responses. Previous studies revealed how ligands with different efficacies activate GPCRs. Here, we investigate how a GPCR activates G-proteins upon binding ligands with different efficacies. We report the cryo-EM structures of β-adrenergic receptor (β-AR) in complex with Gs (GαGβGγ) and a partial agonist or a very weak partial agonist, and compare them to the β-AR-Gs structure in complex with a full agonist. Analyses reveal similar overall complex architecture, with local conformational differences. Cellular functional studies with mutations of β-AR residues show effects on the cellular signaling from β-AR to the cAMP response initiated by the three different ligands, with residue-specific functional differences. Biochemical investigations uncover that the intermediate state complex comprising β-AR and nucleotide-free Gs is more stable when binding a full agonist than a partial agonist. Molecular dynamics simulations support the local conformational flexibilities and different stabilities among the three complexes. These data provide insights into the ligand efficacy in the activation of GPCRs and G-proteins. |
リンク | Nat Commun / PubMed:35835792 / PubMed Central |
手法 | EM (単粒子) |
解像度 | 2.5 - 2.6 Å |
構造データ | EMDB-27328, PDB-8dcr: EMDB-27329, PDB-8dcs: |
化合物 | ChemComp-Y00: ChemComp-P32: |
由来 |
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キーワード | SIGNALING PROTEIN / beta1-adrenergic receptor / dobutamine / partial agonist / cyanopindolol |