8X9S

Identification, structure and agonist design of an androgen membrane receptor.

8X9S の概要

• エントリーDOI: 10.2210/pdb8x9s/pdb
• EMDBエントリー: 38183
• 分子名称: 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, Adhesion G-protein coupled receptor D1, ... (5 entities in total)
• 機能のキーワード: complex, agonist, gpcr, membrane protein
• 由来する生物種: Rattus norvegicus (Norway rat); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 153504.18

構造登録者

Ping, Y.Q.,Yang, Z. (登録日: 2023-12-01, 公開日: 2025-02-12, 最終更新日: 2025-04-09)

主引用文献

Yang, Z.,Ping, Y.Q.,Wang, M.W.,Zhang, C.,Zhou, S.H.,Xi, Y.T.,Zhu, K.K.,Ding, W.,Zhang, Q.Y.,Song, Z.C.,Zhao, R.J.,He, Z.L.,Wang, M.X.,Qi, L.,Ullmann, C.,Ricken, A.,Schoneberg, T.,Gan, Z.J.,Yu, X.,Xiao, P.,Yi, F.,Liebscher, I.,Sun, J.P.
Identification, structure, and agonist design of an androgen membrane receptor.
Cell, 188:1589-, 2025

PubMed Abstract: Androgens, such as 5α-dihydrotestosterone (5α-DHT), regulate numerous functions by binding to nuclear androgen receptors (ARs) and potential unknown membrane receptors. Here, we report that the androgen 5α-DHT activates membrane receptor GPR133 in muscle cells, thereby increasing intracellular cyclic AMP (cAMP) levels and enhancing muscle strength. Further cryoelectron microscopy (cryo-EM) structural analysis of GPR133-Gs in complex with 5α-DHT or its derivative methenolone (MET) reveals the structural basis for androgen recognition. Notably, the presence of the "Φ(F/L)-F-W" and the "F××N/D" motifs, which recognize the hydrophobic steroid core and polar groups, respectively, are common in adhesion GPCRs (aGPCRs), suggesting that many aGPCRs may recognize different steroid hormones. Finally, we exploited in silico screening methods to identify a small molecule, AP503, which activates GPR133 and separates the beneficial muscle-strengthening effects from side effects mediated by AR. Thus, GPR133 represents an androgen membrane receptor that contributes to normal androgen physiology and has important therapeutic potentials.

PubMed: 39884271
DOI: 10.1016/j.cell.2025.01.006

実験手法

ELECTRON MICROSCOPY (3.49 Å)