Label-free sequence-specific DNA sensing using copper-enhanced anodic stripping of purine bases at boron-doped diamond electrodes
Jazyk angličtina Země Spojené státy americké Médium print-electronic
Typ dokumentu časopisecké články, práce podpořená grantem
    PubMed
          
           18321078
           
          
          
    DOI
          
           10.1021/ac7019305
           
          
          
  
    Knihovny.cz E-zdroje
    
  
              
      
- MeSH
 - bor chemie MeSH
 - diamant chemie MeSH
 - DNA-dependentní DNA-polymerasy metabolismus MeSH
 - DNA analýza chemie genetika metabolismus MeSH
 - elektrochemie MeSH
 - elektrody MeSH
 - hydrolýza MeSH
 - kationty chemie MeSH
 - kyseliny chemie MeSH
 - měď chemie MeSH
 - oligonukleotidy chemie MeSH
 - oxidace-redukce MeSH
 - puriny chemie MeSH
 - sekvence nukleotidů MeSH
 - Publikační typ
 - časopisecké články MeSH
 - práce podpořená grantem MeSH
 - Názvy látek
 - bor MeSH
 - diamant MeSH
 - DNA-dependentní DNA-polymerasy MeSH
 - DNA MeSH
 - kationty MeSH
 - kyseliny MeSH
 - měď MeSH
 - oligonukleotidy MeSH
 - purine MeSH Prohlížeč
 - puriny 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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