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Sensitive detection of adenosine triphosphate by exonuclease III-assisted cyclic amplification coupled with surface plasmon resonance enhanced fluorescence based on nanopore
被引:17
|作者:
Li, Xuemei
[1
]
Wang, Yan
[2
]
Luo, Jie
[2
]
Ai, Shiyun
[3
]
机构:
[1] Linyi Univ, Sch Chem & Chem Engn, Linyi 276005, Peoples R China
[2] Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, State Key Lab Base Ecochem Engn, Qingdao 266042, Peoples R China
[3] Shandong Agr Univ, Coll Chem & Mat Sci, Tai An 271018, Shandong, Peoples R China
来源:
SENSORS AND ACTUATORS B-CHEMICAL
|
2016年
/
228卷
基金:
中国国家自然科学基金;
关键词:
Cyclic amplification;
Fluorescence enhancement;
Adenosine triphosphate;
Exonuclease exonuclease III;
Nanopore;
SINGLE-MOLECULE FLUORESCENCE;
DNA;
ATP;
PROBE;
ASSAY;
APTAMER;
NANOPARTICLES;
BIOSENSOR;
PLATFORM;
D O I:
10.1016/j.snb.2016.01.082
中图分类号:
O65 [分析化学];
学科分类号:
070302 ;
081704 ;
摘要:
In traditional bioanalysis with mesoporous silica nanoparticle (MSN) as carrier, fluorescence quenching by encapsulation of fluorescence molecules in the pores was generally used. In the present work, Au nanoparticle@SiO2 mesoporous silica core-shell nanoparticles (AuNP@SiO2 MSN) was synthesized, and surface plasmon resonance enhanced fluorescence localized on nanopore was observed. In-hole fluorescence enhancement by MSN for detection of adenosine 5'-triphosphate (ATP) was developed, on the base of exonuclease III (Exo III)-assisted cyclic amplification and surface plasmon resonance enhanced fluorescence localized on nanopore. Because of the autocatalytic target recycling amplification and the fluorescence enhancement, this designed protocol provided an ultrasensitive detection of ATP down to 0.1 nM level, and can be utilized into cell lysates analysis. (C) 2016 Elsevier B.V. All rights reserved.
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页码:509 / 514
页数:6
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