7EO2

Cryo-EM of Sphingosine 1-phosphate receptor 1 / Gi complex bound to FTY720p

7EO2 の概要

• エントリーDOI: 10.2210/pdb7eo2/pdb
• EMDBエントリー: 31225
• 分子名称: Sphingosine 1-phosphate receptor 1, Guanine nucleotide-binding protein G(i) subunit alpha-1, Guanine nucleotide-binding protein G(I)/G(S)/G(T) subunit beta-1, ... (6 entities in total)
• 機能のキーワード: gpcr, 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: 151143.19

構造登録者

He, Y.,Xu, Z.,Ikuta, T. (登録日: 2021-04-21, 公開日: 2022-01-05, 最終更新日: 2024-11-06)

主引用文献

Xu, Z.,Ikuta, T.,Kawakami, K.,Kise, R.,Qian, Y.,Xia, R.,Sun, M.X.,Zhang, A.,Guo, C.,Cai, X.H.,Huang, Z.,Inoue, A.,He, Y.
Structural basis of sphingosine-1-phosphate receptor 1 activation and biased agonism.
Nat.Chem.Biol., 18:281-288, 2022

PubMed Abstract: Sphingosine-1-phosphate receptor 1 (S1PR1) is a master regulator of lymphocyte egress from the lymph node and an established drug target for multiple sclerosis (MS). Mechanistically, therapeutic S1PR1 modulators activate the receptor yet induce sustained internalization through a potent association with β-arrestin. However, a structural basis of biased agonism remains elusive. Here, we report the cryo-electron microscopy (cryo-EM) structures of G-bound S1PR1 in complex with S1P, fingolimod-phosphate (FTY720-P) and siponimod (BAF312). In combination with functional assays and molecular dynamics (MD) studies, we reveal that the β-arrestin-biased ligands direct a distinct activation path in S1PR1 through the extensive interplay between the PIF and the NPxxY motifs. Specifically, the intermediate flipping of W269 and the retained interaction between F265 and N307 are the key features of the β-arrestin bias. We further identify ligand-receptor interactions accounting for the S1PR subtype specificity of BAF312. These structural insights provide a rational basis for designing novel signaling-biased S1PR modulators.

PubMed: 34937912
DOI: 10.1038/s41589-021-00930-3

実験手法

ELECTRON MICROSCOPY (2.89 Å)