Number of the records: 1  

Label-free detection of canonical DNA bases, uracil and 5-methylcytosine in DNA oligonucleotides using linear sweep voltammetry at a pyrolytic graphite electrode

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    SYSNO ASEP0485557
    Document TypeJ - Journal Article
    R&D Document TypeJournal Article
    Subsidiary JČlánek ve WOS
    TitleLabel-free detection of canonical DNA bases, uracil and 5-methylcytosine in DNA oligonucleotides using linear sweep voltammetry at a pyrolytic graphite electrode
    Author(s) Špaček, Jan (BFU-R) ORCID
    Daňhel, Aleš (BFU-R) RID, ORCID
    Hasoň, Stanislav (BFU-R) RID, ORCID
    Fojta, Miroslav (BFU-R) RID, ORCID
    Number of authors4
    Source TitleElectrochemistry Communications. - : Elsevier - ISSN 1388-2481
    Roč. 82, SEP2017 (2017), s. 34-38
    Number of pages5 s.
    Publication formPrint - P
    Languageeng - English
    CountryNL - Netherlands
    Keywordselectrochemical oxidation ; nucleic-acids ; guanine ; reduction
    Subject RIVEB - Genetics ; Molecular Biology
    OECD categoryBiochemistry and molecular biology
    R&D ProjectsGA16-01625S GA ČR - Czech Science Foundation (CSF)
    EF15_003/0000477 GA MŠMT - Ministry of Education, Youth and Sports (MEYS)
    Institutional supportBFU-R - RVO:68081707
    UT WOS000408359600008
    DOI10.1016/j.elecom.2017.07.013
    AnnotationAn innovative approach to label-free voltammetric analysis of DNA at a pyrolytic graphite electrode (PGE) within a broad range of potentials (from2.0 to + 1.6 V) in an acetate buffer (pH 5) is presented. Using specifically designed DNA nonamers, we demonstrate not only anodic oxidation, but for the first time also cathodic reduction of nucleobases at the PGE. In addition, products of irreversible oxidation/reduction of the parent bases are shown to yield analytically useful, base-specific cathodic/anodic signals, making it possible to distinguish between the canonical bases (adenine, cytosine, guanine and thymine), uracil (U) and 5-methylcytosine (mC) in DNA. Furthermore, selective electrochemical switching off of the redox signals specific to certain nucleobases is presented as a way to resolve overlapping signals. Similarly, newly reported signals corresponding to electrochemically transformed bases can be switched on under specific conditions. This approach can be utilized for fast and facile simultaneous label-free analysis of bases in DNA, including mC and U, and to uncover overlapping signals. This significantly extends the possible applications of PGE in DNA research and (bio) sensor development.
    WorkplaceInstitute of Biophysics
    ContactJana Poláková, polakova@ibp.cz, Tel.: 541 517 244
    Year of Publishing2018
Number of the records: 1  

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