Signal Enhancement for Gene Detection Based on a Redox Reaction of [Fe(CN)6]4- Mediated by Ferrocene at the Terminal of a Peptide Nucleic Acid as a Probe with Hybridization-amenable Conformational Flexibility

  • AOKI Hiroshi
    National Institute of Advanced Industrial Science and Technology (AIST)
  • TAO Hiroaki
    National Institute of Advanced Industrial Science and Technology (AIST)

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Other Title
  • Signal enhancement for gene detection based on a redox reaction of 〔Fe(CN)6〕[4-] mediated by ferrocene at the terminal of a peptide nucleic acid as a probe with hybridization-amenable conformational flexibility

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Abstract

Electrochemically enhanced DNA detection was demonstrated by utilizing the couple of a synthesized ferrocene-terminated peptide nucleic acid (PNA) with a cysteine anchor and a sacrificial electron donor [Fe(CN)6]4-. DNA detection sensors were prepared by modifying a gold electrode surface with a mixed monolayer of the probe PNA and 11-hydroxy-1-undecanethiol (11-HUT), protecting [Fe(CN)6]4- from any unexpected redox reaction. Before hybridization, the terminal ferrocene moiety of the probe was subject to a redox reaction due to the flexible probe structure and, in the presence of [Fe(CN)6]4-, the observed current was amplified based on regeneration of the ferrocene moiety. Hybridization decreased the redox current of the ferrocene. This occurred because hybridization rigidified the probe structure: the ferrocene moiety was then removed from the electrode surface, and the redox reaction of [Fe(CN)6]4- was again prevented. The change in the anodic current before and after hybridization was enhanced 1.75-fold by using the electron donor [Fe(CN)6]4-. Sequence-specific detection of the complementary target DNA was also demonstrated.

Journal

  • Analytical Sciences

    Analytical Sciences 24 (7), 929-933, 2008

    The Japan Society for Analytical Chemistry

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