8JA3

Structure of beta-arrestin1 in complex with C3aRpp

8JA3 の概要

• エントリーDOI: 10.2210/pdb8ja3/pdb
• EMDBエントリー: 36124
• 分子名称: Beta-arrestin-1, C3a anaphylatoxin chemotactic receptor, Fab30 heavy chain, ... (4 entities in total)
• 機能のキーワード: gpcr, arrestin, signaling protein, signaling protein-immune system complex, signaling protein/immune system
• 由来する生物種: Rattus norvegicus (Norway rat); 詳細
• タンパク質・核酸の鎖数: 8
• 化学式量合計: 181013.47

構造登録者

Maharana, J.,Sarma, P.,Yadav, M.K.,Chami, M.,Banerjee, R.,Shukla, A.K. (登録日: 2023-05-05, 公開日: 2023-12-27, 最終更新日: 2024-11-13)

主引用文献

Maharana, J.,Sano, F.K.,Sarma, P.,Yadav, M.K.,Duan, L.,Stepniewski, T.M.,Chaturvedi, M.,Ranjan, A.,Singh, V.,Saha, S.,Mahajan, G.,Chami, M.,Shihoya, W.,Selent, J.,Chung, K.Y.,Banerjee, R.,Nureki, O.,Shukla, A.K.
Molecular insights into atypical modes of beta-arrestin interaction with seven transmembrane receptors.
Science, 383:101-108, 2024

PubMed Abstract: β-arrestins (βarrs) are multifunctional proteins involved in signaling and regulation of seven transmembrane receptors (7TMRs), and their interaction is driven primarily by agonist-induced receptor activation and phosphorylation. Here, we present seven cryo-electron microscopy structures of βarrs either in the basal state, activated by the muscarinic receptor subtype 2 (M2R) through its third intracellular loop, or activated by the βarr-biased decoy D6 receptor (D6R). Combined with biochemical, cellular, and biophysical experiments, these structural snapshots allow the visualization of atypical engagement of βarrs with 7TMRs and also reveal a structural transition in the carboxyl terminus of βarr2 from a β strand to an α helix upon activation by D6R. Our study provides previously unanticipated molecular insights into the structural and functional diversity encoded in 7TMR-βarr complexes with direct implications for exploring novel therapeutic avenues.

PubMed: 38175886
DOI: 10.1126/science.adj3347

実験手法

ELECTRON MICROSCOPY (3.94 Å)