| Literature DB >> 28616667 |
Yunyi Zhang1,2,3, Yongxin Li2, Cuiyun Zhang1,2,3, Qingfeng Zhang2,3, Xinan Huang2, Meiding Yang2,3, Sohail Anjum Shahzad2,4, Kenneth Kam-Wing Lo5, Cong Yu6,7, Shichun Jiang8.
Abstract
A fluorescence turn-on assay for alkaline phosphatase (ALP) activity is developed through the controlled release of polyethyleneimine-capped copper nanoclusters (PEI-capped CuNCs) from the MnO2 nanosheets. In an aqueous solution, the positively charged PEI-capped CuNCs could be adsorbed onto the surface of the negatively charged MnO2 nanosheets. Such adsorption through favorable electrostatic interactions could efficiently quench the nanocluster fluorescence emission via resonance energy transfer from the PEI-capped CuNCs to the MnO2 nanosheets. 2-Phospho-L-ascorbic acid (AAP) could be hydrolyzed to L-ascorbic acid (AA) in the presence of ALP. AA could reduce MnO2 into Mn2+ and trigger the disintegration of the MnO2 nanosheets. As a result, the CuNCs were released and the quenched fluorescence was recovered efficiently. The detection strategy is simple, inexpensive, sensitive, selective, with low toxicity, and has better biocompatibility. The newly fabricated biosensor for ALP activity will potentially make it a robust candidate for numerous biological and biomedical applications.Entities:
Keywords: Alkaline phosphatase; Cu nanoclusters; Enzyme activity; Fluorescence assay; MnO2 nanosheets
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Year: 2017 PMID: 28616667 DOI: 10.1007/s00216-017-0420-9
Source DB: PubMed Journal: Anal Bioanal Chem ISSN: 1618-2642 Impact factor: 4.142