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Sensitive immobilization-free electrochemical DNA sensor based on isothermal circular strand displacement polymerization reaction
被引:60
作者:
Xuan, Feng
[2
]
Luo, Xiaoteng
[2
]
Hsing, I-Ming
[1
,2
]
机构:
[1] Hong Kong Univ Sci & Technol, Div Biomed Engn, Kowloon, Hong Kong, Peoples R China
[2] Hong Kong Univ Sci & Technol, Dept Chem & Biomol Engn, Kowloon, Hong Kong, Peoples R China
关键词:
Immobilization-free;
Electrochemical;
DNA sensor;
Strand displacement;
HYBRIDIZATION DETECTION;
MOLECULAR BEACONS;
NUCLEIC-ACID;
AMPLIFICATION;
MICROARRAYS;
BIOSENSOR;
D O I:
10.1016/j.bios.2012.02.054
中图分类号:
Q6 [生物物理学];
学科分类号:
071011 ;
摘要:
A highly sensitive electrochemical DNA sensor that requires no probe immobilization has been developed based on a target recycling mechanism utilizing a DNA polymerase with a strand displacement activity. The electrochemical detection is realized by taking advantage of the difference in diffusivity between a free ferrocene-labeled peptide nucleic acid (Fc-PNA) and a Fc-PNA hybridized with a complementary DNA, while the DNA polymerase-assisted target recycling leads to signal generation and amplification. The hybridization of the target DNA opens up a stem-loop template DNA with the Fc-PNA hybridized to its extruded 5' end and allows a DNA primer to anneal and be extended by the DNA polymerase, which results in sequential displacement of the target DNA and the Fc-PNA from the template DNA. The displaced target DNA will hybridize with another template DNA, triggering another round of primer extension and strand displacement. The released Fc-PNA, due to its neutral backbone, has much higher diffusivity towards a negatively charged electrode, compared to that when it is hybridized with a negatively charged DNA. Therefore, a significantly enhanced signal of Fc can be observed. The outstanding sensitivity and simplicity make this approach a promising candidate for next-generation electrochemical DNA sensing technologies. (C) 2012 Elsevier B.V. All rights reserved.
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页码:230 / 234
页数:5
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