A highly selective naphthalimide-based ratiometric fluorescent probe for the recognition of tyrosinase and cellular imaging

被引:30
|
作者
Sidhu, Jagpreet Singh [1 ]
Singh, Ashutosh [2 ]
Garg, Neha [2 ]
Kaur, Navneet [3 ]
Singh, Narinder [1 ]
机构
[1] Indian Inst Technol Ropar, Dept Chem, Rupnagar 140001, Punjab, India
[2] Indian Inst Technol Mandi, Sch Basic Sci, Mandi 175005, Himachal Prades, India
[3] Panjab Univ, Dept Chem, Chandigarh 160014, India
关键词
LARGE STOKES SHIFT; BIOCATALYTIC TRANSFORMATIONS; CARBON DOTS; SENSOR; CELLS; INHIBITORS; ASSAY; PET; PEROXYNITRITE; NANOPARTICLES;
D O I
10.1039/c8an01136b
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Tyrosinase is polyphenolic oxidase enzyme associated with the progression of various diseases. Therefore, for the recognition of tyrosinase, naphthalimide-based ratiometric fluorescent sensor probe was designed and synthesized. 3-Hydroxyphenyl, as the substrate unit for the enzyme, is an important feature of this design, which avoids the interference of other bio-analytes for the recognition of tyrosinase. When the sensor probe was excited at 425 nm, an intense blue emission band emerged at 467 nm. However, upon the addition of tyrosinase to the probe solution, the monophenolic unit oxidized to o-dihydroxy and consequently released the 4-aminonaphthalimide unit. As the oxidation reaction proceeded, the fluorescence emission at 535 nm started to increase gradually with an increase in the concentration of enzyme. Therefore, the sensor probe gives the ratiometric changes via fluorescence spectroscopy. The probe affords high selectivity and sensitivity to tyrosinase with a detection limit of 0.2 U mL(-1). Furthermore, live cell images were recorded to assay the endogenous enzyme in A375 cells, which also show a dual color change in the presence of the L3 probe.
引用
收藏
页码:4476 / 4483
页数:8
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