Abstract
Tyrosinase is a key enzyme in melanin biosynthesis and its serum level is an important biomarker for some dermatoses such as vitiligo and melanoma. Thus, a sensitive and facile assay for tyrosinase activity is in urgent demands. Lucigenin is a well-known chemiluminescent luminophore, but has been rarely been employed for fluorescence detection. In this work, a facile method to detect tyrosinase activity based on lucigenin fluorescence has been reported for the first time. When tyrosinase was mixed with tyrosine, tyrosine was oxidized to generate melanin-like polymers which can effectively quench the fluorescence of lucigenin. A linear range of tyrosinase from 0.25 to 25 μg/mL was obtained with detection limit of 0.2 μg/mL. In addition, a useful platform for screening potential tyrosinase inhibitors was constructed based on the proposed system. The linear range is from 2.5 to 62.5 μg/mL and the detection limit is as low as 1.0 μg/mL for kojic acid, a typical tyrosinase inhibitor.
Original language | English |
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Pages (from-to) | 41-45 |
Number of pages | 5 |
Journal | Sensors and Actuators, B: Chemical |
Volume | 280 |
DOIs | |
Publication status | Published - Feb 1 2019 |
Externally published | Yes |
Keywords
- Drug screening
- Fluorescent biosensor
- Inhibitors
- Kojic acid
- Lucigenin
- Tyrosinase
ASJC Scopus subject areas
- Electronic, Optical and Magnetic Materials
- Instrumentation
- Condensed Matter Physics
- Surfaces, Coatings and Films
- Metals and Alloys
- Electrical and Electronic Engineering
- Materials Chemistry