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.
引用
收藏
页数:6
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