Label-free sequence-specific DNA sensing using copper-enhanced anodic stripping of purine bases at boron-doped diamond electrodes
Language English Country United States Media print-electronic
Document type Journal Article, Research Support, Non-U.S. Gov't
PubMed
18321078
DOI
10.1021/ac7019305
Knihovny.cz E-resources
- MeSH
- Boron chemistry MeSH
- Diamond chemistry MeSH
- DNA-Directed DNA Polymerase metabolism MeSH
- DNA analysis chemistry genetics metabolism MeSH
- Electrochemistry MeSH
- Electrodes MeSH
- Hydrolysis MeSH
- Cations chemistry MeSH
- Acids chemistry MeSH
- Copper chemistry MeSH
- Oligonucleotides chemistry MeSH
- Oxidation-Reduction MeSH
- Purines chemistry MeSH
- Base Sequence MeSH
- Publication type
- Journal Article MeSH
- Research Support, Non-U.S. Gov't MeSH
- Names of Substances
- Boron MeSH
- Diamond MeSH
- DNA-Directed DNA Polymerase MeSH
- DNA MeSH
- Cations MeSH
- Acids MeSH
- Copper MeSH
- Oligonucleotides MeSH
- purine MeSH Browser
- Purines MeSH
Stripping voltammetric determination of purine bases in the presence of copper ions at mercury, amalgam, or carbon-based electrodes has recently been utilized in analysis of DNA or synthetic oligodeoxynucleotides (ODNs). Here we report on copper-enhanced label-free anodic stripping detection of guanine and adenine bases in acid-hydrolyzed DNA at anodically oxidized boron-doped diamond electrode (AO-BDDE). The AO-BDDE was successfully applied in a three-electrode microcell in which an approximately 50 microL drop of the analyte solution can be efficiently stirred during the accumulation step by streaming of an inert gas. Accelerated mass transport due to the solution motion in the presence of copper resulted in enhancement of the guanine oxidation signal by about 2 orders of magnitude (compared to accumulation of the analyte from still solution not containing copper), allowing an easy detection of approximately 25 fmol of the ODNs. The proposed technique is shown to be suitable for a determination of purine (particularly guanine) content in DNA samples. Applications of the technique in magnetic bead-based DNA assays (such as hybridization with DNA sequences exhibiting asymmetrical distribution of purine/pyrimidine nucleotides between the complementary strands or monitoring of amplification of specific DNA fragments in a duplex polymerase chain reaction) are demonstrated.
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