Probing phosphatase activity using redox active nanoparticles: A novel colorimetric approach for the detection of enzyme activity

被引:74
作者
Hayat, Akhtar [1 ,2 ]
Bulbul, Gonca [1 ]
Andreescu, Silvana [1 ]
机构
[1] Clarkson Univ, Dept Chem & Biomol Sci, Potsdam, NY 13676 USA
[2] COMSATS Inst Informat Technol CIIT, IRCBM, Lahore, Pakistan
基金
美国国家科学基金会;
关键词
Phosphatase; Assay; Redox active nanoparticles; Nanoceria; Phosphatase substrates; Charge transfer complexes; ALKALINE-PHOSPHATASE; GOLD NANOPARTICLES; CERIA NANOPARTICLES; ASSAY; SUBSTRATE;
D O I
10.1016/j.bios.2014.01.003
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A new calorimetric assay for the detection of alkaline phosphatase (ALP) activity is reported based on the surface reactivity and optical properties of redox active nanoparticles of cerium oxide, or nanoceria. The method takes advantage of nanoceria color changes after interaction with products of the ALP catalyzed reaction, resulting in charge transfer complexes with very strong absorption characteristics. The developed assay is easy-to-use, robust and cost effective and does not involve labeled reagents, secondary enzymes or soluble dyes. Hydrolytic products of more stable substrates (catechol monophosphate, ascorbic 2-phosphate and hydroquinone diphosphate) that could previously not be used in ALP assays can be conveniently colorimetrically detected with this assay. A detection limit of 0.04 U/L ALP with a linear range up to 2 U/L was obtained with ascorbic 2-phosphate substrate. The proposed assay can eliminate multistep procedures and minimize problems associated with the poor stability of substrates and enzyme labels of conventional ALP assays. The assay has been adapted to a paper platform and has demonstrated functionality for ALP detection in human serum. This sensing concept can find wide applications as a general approach for improving sensitivity and simplifying detection schemes of colorimetric bioassays, e.g. enzyme, gene, immuno and aptamer assays and related affinity sensing methods. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:334 / 339
页数:6
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