A fluorometric displacement assay for adenosine triphosphate using layered cobalt(II) double hydroxide nanosheets

被引:7
|
作者
Liu, Jingjing [1 ,2 ,3 ]
Xu, Xiao [1 ,2 ]
Chen, Zhitao [3 ]
Li, Renfu [1 ,2 ]
Kang, Longtian [1 ,2 ]
Yao, Jiannian [4 ]
机构
[1] Chinese Acad Sci, CAS Key Lab Design & Assembly Funct Nanostruct, Fujian Inst Res Struct Matter, Fuzhou 350002, Fujian, Peoples R China
[2] Chinese Acad Sci, Fujian Prov Key Lab Nanomat, Fujian Inst Res Struct Matter, Fuzhou 350002, Fujian, Peoples R China
[3] Fujian Normal Univ, Sch Ocean & Biochem Engn, Fuqing Branch, Fuqing 350300, Fujian, Peoples R China
[4] Chinese Acad Sci, BNLMS, Inst Chem, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
Dye-labeled DNA; Phosphate-containing metabolites; Two-dimensional layered materials; Quenching mechanism; Serum analysis; SIGNAL AMPLIFICATION; QUANTUM DOTS; ATP; NANOCONES; APTAMER; PROBES; DNA;
D O I
10.1007/s00604-019-3371-3
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A turn-on fluorometric method is described for the determination of adenosine-5-triphosphate (ATP). It is based on the displacement of a dye-labeled oligonucleotide from a cobalt(II) based layered double hydroxide (LDH). Due to the electrostatic and ligand exchange interaction, the FAM-labeled DNA is readily adsorbed on the LDH. This leads to complete and fast quenching of the green fluorescence of the label. However, on addition of ATP, the DNA is detached from the LDH because of the stronger affinity of ATP for LDH. This results in the restoration of the green fluorescence. The effect was used to design a sensitive assay that has a linear response in the 0.5-100M ATP concentration range and a 0.23M lower detection limit. It was applied to the determination of ATP in spiked serum samples.
引用
收藏
页数:7
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