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基于荧光共振能量转移的荧光比率探针用于活细胞内源性硫化氢的快速检测。

FRET-based fluorescent ratiometric probes for the rapid detection of endogenous hydrogen sulphide in living cells.

机构信息

State Key Laboratory of Coordination Chemistry, Coordination ChemistryInstitute, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210023, P. R. China.

出版信息

Analyst. 2020 Jun 21;145(12):4233-4238. doi: 10.1039/d0an00531b. Epub 2020 May 22.

Abstract

Real-time monitoring of hydrogen sulphide (HS) level change is of crucial importance for the study of its complicated roles in physiology. Herein, we developed a FRET strategy for designing ratiometric fluorescent HS sensors. A coumarin-derived merocyanine fluorophore was selected as the acceptor, and two green-light-emission fluorophores were introduced as donors. The sensing mechanism was based on tuning the FRET efficiency, and the free sensors exhibited strong near-infrared emission at 665 nm due to the FRET process. The nucleophilic addition of HS to the imide carbon disrupts the large conjugation system of merocyanine, which induces a dramatic loss of its absorption; thus, the FRET process gets blocked, and the green emission is increased. In the aqueous solution, both the probes, NBD-CMC and Nap-CMC, showed ratiometric HS sensing behaviour, fast response, and high selectivity and sensitivity. Moreover, probe NBD-CMC was successfully applied to monitor the fluctuation of exogenously and endogenously generated HS in HepG-2 cells.

摘要

实时监测硫化氢 (HS) 水平的变化对于研究其在生理学中的复杂作用至关重要。为此,我们开发了一种用于设计比率型荧光 HS 传感器的 FRET 策略。选择香豆素衍生的次甲基菁荧光团作为受体,并引入两个绿光发射荧光团作为供体。该传感机制基于调节 FRET 效率,由于 FRET 过程,游离传感器在 665nm 处显示出强的近红外发射。HS 的亲核加成到酰亚胺碳上破坏了次甲基菁的大共轭体系,导致其吸收急剧损失;因此,FRET 过程被阻断,绿色发射增加。在水溶液中,探针 NBD-CMC 和 Nap-CMC 均表现出比率型 HS 传感行为,具有快速响应、高选择性和灵敏度。此外,探针 NBD-CMC 成功应用于监测 HepG-2 细胞中外源性和内源性产生的 HS 的波动。

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