化学
阿片受体
(+)-纳洛酮
配体(生物化学)
表面等离子共振
荧光
配体结合分析
兴奋剂
类阿片
受体
生物物理学
敌手
组合化学
立体化学
纳米技术
生物化学
物理
生物
材料科学
量子力学
纳米颗粒
作者
Yan Jia,Lili Xu,Lancheng Wang,Yan Ke,Jieru Chen,Ping Xu,Bin Di,F. Yan,Chi Hu
标识
DOI:10.1016/j.aca.2023.341220
摘要
With the aggravated burden of opioid use disorder spreading worldwide, demands for new forms of opioid receptor agonist/antagonist constitute immense research interest. The Mu-opioid receptor (MOR) is currently in the spotlight on account of its general involvement in opioid-induced antinociception, tolerance and dependence. MOR binding assay, however, is often complicated by difficulty in MOR separation and purification, as well as the tedious procedure in standard biolayer interferometry and surface plasmon resonance measurements. To this end, we present TPE2N as a light-up fluorescent probe for MOR, which exhibits satisfactory performance in both live cells and lysates. TPE2N was elaborately designed based on the synergistic effect of twisted intramolecular charge-transfer and aggregation-induced emission by incorporating a tetraphenylethene unit to emit strong fluorescence in a restrained environment upon binding with MOR through the naloxone pharmacore. The developed assay enabled high-throughput screening of a compound library, and successfully identified three ligands as lead compounds for further development.
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