6LUQ

Haloperidol bound D2 dopamine receptor structure inspired discovery of subtype selective ligands

6LUQ の概要

• エントリーDOI: 10.2210/pdb6luq/pdb
• 分子名称: chimera of D(2) dopamine receptor and Endolysin, 4-[4-(4-chlorophenyl)-4-hydroxypiperidin-1-yl]-1-(4-fluorophenyl)butan-1-one, OLEIC ACID, ... (4 entities in total)
• 機能のキーワード: gpcr, dopamine receptor, haloperidol, d2 dopamine receptor, membrane protein
• 由来する生物種: Homo sapiens (Human); 詳細
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 50385.11

構造登録者

Fan, L.,Tan, L.,Chen, Z.,Qi, J.,Nie, F.,Luo, Z.,Cheng, J.,Wang, S. (登録日: 2020-01-30, 公開日: 2020-03-04, 最終更新日: 2024-11-06)

主引用文献

Fan, L.,Tan, L.,Chen, Z.,Qi, J.,Nie, F.,Luo, Z.,Cheng, J.,Wang, S.
Haloperidol bound D2dopamine receptor structure inspired the discovery of subtype selective ligands.
Nat Commun, 11:1074-1074, 2020

PubMed Abstract: The D dopamine receptor (DRD2) is one of the most well-established therapeutic targets for neuropsychiatric and endocrine disorders. Most clinically approved and investigational drugs that target this receptor are known to be subfamily-selective for all three D-like receptors, rather than subtype-selective for only DRD2. Here, we report the crystal structure of DRD2 bound to the most commonly used antipsychotic drug, haloperidol. The structures suggest an extended binding pocket for DRD2 that distinguishes it from other D-like subtypes. A detailed analysis of the structures illuminates key structural determinants essential for DRD2 activation and subtype selectivity. A structure-based and mechanism-driven screening combined with a lead optimization approach yield DRD2 highly selective agonists, which could be used as chemical probes for studying the physiological and pathological functions of DRD2 as well as promising therapeutic leads devoid of promiscuity.

PubMed: 32103023
DOI: 10.1038/s41467-020-14884-y

実験手法

X-RAY DIFFRACTION (3.1 Å)