Abstract
A systematic study of the amplified optical detection of DNA by Mg 2+-dependent DNAzyme subunits is described. The use of two DNAzyme subunits and the respective fluorophore/quencher-modified substrate allows the detection of the target DNA with a sensitivity corresponding to 1 × 10 -9 M. The use of two functional hairpin structures that include the DNAzyme subunits in a caged, inactive configuration leads, in the presence of the target DNA, to the opening of one of the hairpins and to the activation of an autonomous cross-opening process of the two hairpins, which affords polymer DNA wires consisting of the Mg 2+-dependent DNAzyme subunits. This amplification paradigm leads to the analysis of the target DNA with a sensitivity corresponding to 1 × 10 -14 M. The amplification mixture composed of the two hairpins can be implemented as a versatile sensing platform for analyzing any gene in the presence of the appropriate hairpin probe. This is exemplified with the detection of the BRCA1 oncogene.
| Original language | English |
|---|---|
| Pages (from-to) | 17149-17151 |
| Number of pages | 3 |
| Journal | Journal of the American Chemical Society |
| Volume | 133 |
| Issue number | 43 |
| DOIs | |
| State | Published - 2 Nov 2011 |
Fingerprint
Dive into the research topics of 'Amplified analysis of DNA by the autonomous assembly of polymers consisting of DNAzyme wires'. Together they form a unique fingerprint.Cite this
- APA
- Author
- BIBTEX
- Harvard
- Standard
- RIS
- Vancouver