8TZI

Human equilibrative nucleoside transporter-1, JH-ENT-01 bound

8TZI の概要

• エントリーDOI: 10.2210/pdb8tzi/pdb
• 分子名称: Equilibrative nucleoside transporter 1, (2R)-2,3-dihydroxypropyl (9Z)-octadec-9-enoate, 3-(4-{3-[(3,4,5-trimethoxybenzoyl)oxy]propyl}-1,4-diazepan-1-yl)propyl 3,4-dimethoxy-5-[(4-nitrophenyl)methoxy]benzoate, ... (4 entities in total)
• 機能のキーワード: adenosine transport, adenosine reuptake inhibitor, nucleoside, hent1, equilibrative nucleoside transporter, slc29, transport protein-inhibitor complex, transport protein/inhibitor
• 由来する生物種: Homo sapiens (human)
• タンパク質・核酸の鎖数: 1
• 化学式量合計: 51728.73

構造登録者

Wright, N.J.,Lee, S.Y. (登録日: 2023-08-26, 公開日: 2024-08-28, 最終更新日: 2026-04-15)

主引用文献

Wright, N.J.,Matsuoka, Y.,Park, H.,He, W.,Webster, C.G.,Furutani, K.,Fedor, J.G.,McGinnis, A.,Zhao, Y.,Chen, O.,Bang, S.,Fan, P.,Spasojevic, I.,Hong, J.,Ji, R.R.,Lee, S.Y.
Design of an equilibrative nucleoside transporter subtype 1 inhibitor for pain relief.
Nat Commun, 15:10738-10738, 2024

PubMed Abstract: The current opioid crisis urgently calls for developing non-addictive pain medications. Progress has been slow, highlighting the need to uncover targets with unique mechanisms of action. Extracellular adenosine alleviates pain by activating the adenosine A1 receptor (A1R). However, efforts to develop A1R agonists have faced obstacles. The equilibrative nucleoside transporter subtype 1 (ENT1) plays a crucial role in regulating adenosine levels across cell membranes. We postulate that ENT1 inhibition may enhance extracellular adenosine levels, potentiating endogenous adenosine action at A1R and leading to analgesic effects. Here, we modify the ENT1 inhibitor dilazep based on its complex X-ray structure and show that this modified inhibitor reduces neuropathic and inflammatory pain in animal models while dilazep does not. Notably, our ENT1 inhibitor surpasses gabapentin in analgesic efficacy in a neuropathic pain model. Additionally, our inhibitor exhibits less cardiac side effect than dilazep via systemic administration and shows no side effects via local/intrathecal administration. ENT1 is colocalized with A1R in mouse and human dorsal root ganglia, and the analgesic effect of our inhibitor is linked to A1R. Our studies reveal ENT1 as a therapeutic target for analgesia, highlighting the promise of rationally designed ENT1 inhibitors for non-opioid pain medications.

PubMed: 39737929
DOI: 10.1038/s41467-024-54914-7

実験手法

X-RAY DIFFRACTION (2.7 Å)