8EIT

Structure of FFAR1-Gq complex bound to DHA

8EIT の概要

• エントリーDOI: 10.2210/pdb8eit/pdb
• EMDBエントリー: 28164
• 分子名称: A modified Guanine nucleotide-binding protein G(q) subunit alpha, 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, ... (6 entities in total)
• 機能のキーワード: ffar1, ffas, diabetes, cryoem, membrane protein
• 由来する生物種: Homo sapiens (human); 詳細
• タンパク質・核酸の鎖数: 5
• 化学式量合計: 163750.99

構造登録者

Kumari, P.,Inoue, A.,Chapman, K.,Lian, P.,Rosenbaum, D.M. (登録日: 2022-09-15, 公開日: 2023-05-24, 最終更新日: 2025-05-28)

主引用文献

Kumari, P.,Inoue, A.,Chapman, K.,Lian, P.,Rosenbaum, D.M.
Molecular mechanism of fatty acid activation of FFAR1.
Proc.Natl.Acad.Sci.USA, 120:e2219569120-e2219569120, 2023

PubMed Abstract: FFAR1 is a G-protein-coupled receptor (GPCR) that responds to circulating free fatty acids to enhance glucose-stimulated insulin secretion and release of incretin hormones. Due to the glucose-lowering effect of FFAR1 activation, potent agonists for this receptor have been developed for the treatment of diabetes. Previous structural and biochemical studies of FFAR1 showed multiple sites of ligand binding to the inactive state but left the mechanism of fatty acid interaction and receptor activation unknown. We used cryo-electron microscopy to elucidate structures of activated FFAR1 bound to a G mimetic, which were induced either by the endogenous FFA ligand docosahexaenoic acid or γ-linolenic acid and the agonist drug TAK-875. Our data identify the orthosteric pocket for fatty acids and show how both endogenous hormones and synthetic agonists induce changes in helical packing along the outside of the receptor that propagate to exposure of the G-protein-coupling site. These structures show how FFAR1 functions without the highly conserved "DRY" and "NPXXY" motifs of class A GPCRs and also illustrate how the orthosteric site of a receptor can be bypassed by membrane-embedded drugs to confer full activation of G protein signaling.

PubMed: 37216523
DOI: 10.1073/pnas.2219569120

実験手法

ELECTRON MICROSCOPY (2.8 Å)