Abstract
We have developed a selective, sensitive, and re-usable electrochemical sensor for Hg2+ ion detection. This sensor is based on the Hg 2+-induced conformational change of a single-stranded DNA (ssDNA) which involves an electroactive, ferrocene-labeled DNA hairpin structure and provides strategically the selective binding of a thymine-thymine mismatch for the Hg2+ ion. The ferrocene-labeled DNA is self-assembled through S-Au bonding on a polycrystalline gold electrode surface and the surface blocked with 3-mercapto-1-propanol to form a mixed monolayer. The modified electrode showed a voltammetric signal due to a one-step redox reaction of the surface-confined ferrocenyl moiety. The 'signal-on' upon mercury binding could be attributed to a change in the conformation of ferrocene-labeled DNA from an open structure to a restricted hairpin structure. The differential pulse voltammetry (DPV) of the modified electrode showed a linear response of the ferrocene oxidation signal with increase of Hg2+ concentration in the range between 0.1 and 2 M with a detection limit of 0.1 M. The molecular beacon mercury(ii) ion sensor was amenable to regeneration by simply unfolding the ferrocene-labeled DNA in 10 M cysteine, and could be regenerated with no loss in signal gain upon subsequent mercury(ii) ion binding.
Original language | English |
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Pages (from-to) | 1857-1862 |
Number of pages | 6 |
Journal | Analyst |
Volume | 134 |
Issue number | 9 |
DOIs | |
Publication status | Published - 2009 |
ASJC Scopus subject areas
- Analytical Chemistry
- Biochemistry
- Environmental Chemistry
- Spectroscopy
- Electrochemistry