7E2X

Apo serotonin 1A (5-HT1A) receptor-Gi protein complex

7E2X の概要

• エントリーDOI: 10.2210/pdb7e2x/pdb
• EMDBエントリー: 30971
• 分子名称: Guanine nucleotide-binding protein G(i) subunit alpha-1, 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, ... (8 entities in total)
• 機能のキーワード: serotonin, 5-ht1a, gpcr, complex, g protein, gi, signaling protein
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 4
• 化学式量合計: 152089.90

構造登録者

Xu, P.,Huang, S.,Zhang, H.,Mao, C.,Zhou, X.E.,Shen, D.D.,Jiang, Y.,Zhang, Y.,Xu, H.E. (登録日: 2021-02-07, 公開日: 2021-04-14, 最終更新日: 2024-10-23)

主引用文献

Xu, P.,Huang, S.,Zhang, H.,Mao, C.,Zhou, X.E.,Cheng, X.,Simon, I.A.,Shen, D.D.,Yen, H.Y.,Robinson, C.V.,Harpsoe, K.,Svensson, B.,Guo, J.,Jiang, H.,Gloriam, D.E.,Melcher, K.,Jiang, Y.,Zhang, Y.,Xu, H.E.
Structural insights into the lipid and ligand regulation of serotonin receptors.
Nature, 592:469-473, 2021

PubMed Abstract: Serotonin, or 5-hydroxytryptamine (5-HT), is an important neurotransmitter that activates the largest subtype family of G-protein-coupled receptors. Drugs that target 5-HT, 5-HT, 5-HT and other 5-HT receptors are used to treat numerous disorders. 5-HT receptors have high levels of basal activity and are subject to regulation by lipids, but the structural basis for the lipid regulation and basal activation of these receptors and the pan-agonism of 5-HT remains unclear. Here we report five structures of 5-HT receptor-G-protein complexes: 5-HT in the apo state, bound to 5-HT or bound to the antipsychotic drug aripiprazole; 5-HT bound to 5-HT; and 5-HT in complex with a 5-HT- and 5-HT-selective agonist, BRL-54443. Notably, the phospholipid phosphatidylinositol 4-phosphate is present at the G-protein-5-HT interface, and is able to increase 5-HT-mediated G-protein activity. The receptor transmembrane domain is surrounded by cholesterol molecules-particularly in the case of 5-HT, in which cholesterol molecules are directly involved in shaping the ligand-binding pocket that determines the specificity for aripiprazol. Within the ligand-binding pocket of apo-5-HT are structured water molecules that mimic 5-HT to activate the receptor. Together, our results address a long-standing question of how lipids and water molecules regulate G-protein-coupled receptors, reveal how 5-HT acts as a pan-agonist, and identify the determinants of drug recognition in 5-HT receptors.

PubMed: 33762731
DOI: 10.1038/s41586-021-03376-8

実験手法

ELECTRON MICROSCOPY (3 Å)