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Enzyme-free colorimetric detection systems based on the DNA strand displacement competition reaction
被引:2
作者:
Zhang, Z.
[1
,2
]
Birkedal, V.
[1
]
Gothelf, K. V.
[1
]
机构:
[1] Aarhus Univ, Ctr DNA Nanotechnol CDNA, Interdisciplinary Nanosci Ctr iNANO, DK-8000 Aarhus C, Denmark
[2] Yale Univ, Nanobiol Inst, West Haven, CT 06516 USA
基金:
新加坡国家研究基金会;
关键词:
DNA;
sensor;
strand displacement;
aptamer;
G-quadruplex;
AMPLIFIED DETECTION;
NUCLEIC-ACIDS;
APTAMERS;
SENSORS;
NANOSTRUCTURES;
MOLECULES;
DNAZYME;
COMPLEX;
D O I:
10.1088/1367-2630/18/5/055002
中图分类号:
O4 [物理学];
学科分类号:
0702 ;
摘要:
The strand displacement competition assay is based on the dynamic equilibrium of the competitive hybridization of two oligonucleotides (A and B) to a third oligonucleotide (S). In the presence of an analyte that binds to a specific affinity-moiety conjugated to strand B, the equilibrium shifts, which can be detected by a shift in the fluorescence resonance energy transfer signal between dyes attached to theDNAstrands. In the present study we have integrated an ATP aptamer in the strand B and demonstrated the optical detection of ATP. Furthermore we explore a new readout method using a split G-quadruplex DNAzyme for colorimetric readout of the detection of streptavidin by the naked eye. Finally, we integrate the whole G-quadruplex DNAzyme system in a singleDNAstrand and show that it is applicable to colorimetric detection.
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页数:6
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