8JIL

Cryo-EM structure of niacin bound ketone body receptor HCAR2-Gi signaling complex

8JIL の概要

• エントリーDOI: 10.2210/pdb8jil/pdb
• EMDBエントリー: 36317 36494 36495 36507
• 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, Guanine nucleotide-binding protein G(i) subunit alpha-1, ... (8 entities in total)
• 機能のキーワード: complex, agonist, 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: 162597.61

構造登録者

Zhao, C.,Tian, X.W.,Liu, Y.,Cheng, L.,Yan, W.,Shao, Z.H. (登録日: 2023-05-26, 公開日: 2023-09-06, 最終更新日: 2024-10-23)

主引用文献

Zhao, C.,Wang, H.,Liu, Y.,Cheng, L.,Wang, B.,Tian, X.,Fu, H.,Wu, C.,Li, Z.,Shen, C.,Yu, J.,Yang, S.,Hu, H.,Fu, P.,Ma, L.,Wang, C.,Yan, W.,Shao, Z.
Biased allosteric activation of ketone body receptor HCAR2 suppresses inflammation.
Mol.Cell, 83:3171-, 2023

PubMed Abstract: Hydroxycarboxylic acid receptor 2 (HCAR2), modulated by endogenous ketone body β-hydroxybutyrate and exogenous niacin, is a promising therapeutic target for inflammation-related diseases. HCAR2 mediates distinct pathophysiological events by activating G protein or β-arrestin effectors. Here, we characterize compound 9n as a G-biased allosteric modulator (BAM) of HCAR2 and exhibit anti-inflammatory efficacy in RAW264.7 macrophages via a specific HCAR2-G pathway. Furthermore, four structures of HCAR2-G complex bound to orthosteric agonists (niacin or monomethyl fumarate), compound 9n, and niacin together with compound 9n simultaneously reveal a common orthosteric site and a unique allosteric site. Combined with functional studies, we decipher the action framework of biased allosteric modulation of compound 9n on the orthosteric site. Moreover, co-administration of compound 9n with orthosteric agonists could enhance anti-inflammatory effects in the mouse model of colitis. Together, our study provides insight to understand the molecular pharmacology of the BAM and facilitates exploring the therapeutic potential of the BAM with orthosteric drugs.

PubMed: 37597514
DOI: 10.1016/j.molcel.2023.07.030

実験手法

ELECTRON MICROSCOPY (3.5 Å)