Electrochemistry Of DNA Research Articles

Nitrogen doped chiral carbonaceous nanotube for ultrasensitive DNA direct electrochemistry, DNA hybridization and damage study

In the interest of developing novel electrocatalyst for high performance DNA biosensing, with distinctive chiral double helix nanostructure, nitrogen doped chiral carbonaceous nanotube (Chiral-CNT) was employed for ultrasensitive label-free DNA biosensing research. Chiral-CNT can quantitative detection of four DNA bases with high sensitivity and selectivity. Without any prehydrolysis and labeling process, direct electrochemistry of single-stranded DNA and double-stranded DNA, qualitative and quantitative detection of DNA hybridization (low detection limit: 0.0268 g L−1) were realized. Moreover, sensitive detection of DNA damage induced by fenton reagent was also realized with low detection limit of 0.0350 mg mL−1 and high sensitivity of 7.42 μA mg−1 mL. The high biosensing performance attributes to the unique chiral structure of Chiral-CNT, leads to efficient interreaction between Chiral-CNT and DNA molecule.

Application in Electrochemistry of Graphene-Modified Electrodes

Due to its unique physicochemical properties, graphene has received increasing attention. This article selectively reviews the application of graphene for direct electrochemistry of enzymes, small biomolecules, DNA sensing, and environmental analysis. Graphene oxide (GO) and reduced graphene oxide (RGO) have been used as sensors for gases and heavy metal ions. In all cases, the sensors performed well, proving to be highly sensitive, selective, and stable. Keywords: Graphene, Electrochemical performances, Modified electrodes.

Ordered mesoporous carbon modified carbon ionic liquid electrode for the electrochemical detection of double-stranded DNA

In this paper the direct electrochemistry of double-stranded DNA (dsDNA) was investigated on ordered mesoporous carbon (OMC) modified carbon ionic liquid electrode (CILE). CILE was prepared by mixing graphite powder with 1-ethyl-3-methylimidazolium ethylsulphate ([EMIM]EtOSO 3) and liquid paraffin. A stable OMC film was formed on the surface of CILE with the help of Nafion to get a modified electrode denoted as Nafion-OMC/CILE. Due to the specific characteristics of OMC and IL present on the electrode surface, the fabricated electrode showed good electrochemical performances to different electroactive molecules. The electrochemical responses of dsDNA were carefully investigated on this electrode with two irreversible oxidation peak appeared at +1.250 V and +0.921 V (vs. SCE), which was corresponding to the oxidation of adenine and guanine residues in dsDNA structure. The electrochemical behaviors of dsDNA were carefully investigated on the Nafion-OMC/CILE. Experimental results indicated that the electron transfer rate was promoted with the increase of the oxidation peak current and the decrease of the oxidation peak potential, which was due to the electrocatalytic ability of OMC on the electrode surface. Under the optimal conditions the oxidation peak current increased with dsDNA concentration in the range of 10.0–600.0 μg mL −1 by differential pulse voltammetry (DPV) with the detection limit of 1.2 μg mL −1 (3 σ).

From DC polarographic presodium wave of proteins to electrochemistry of biomacromolecules

History of electrochemistry of proteins and nucleic acids is briefly reviewed. The ability of proteins to catalyze hydrogen evolution at Hg electrodes was discovered almost 80 years ago in J. Heyrovský’s laboratory. This phenomenon was not sufficiently appreciated for several decades. Recently it has been shown that using constant current chronopotentiometric stripping (CPS) with hanging mercury drop, solid amalgam or Hg-film electrodes the CPS peak H is obtained with nanomolar concentrations of peptides and proteins. This peak is derived from the presodium wave but it has some new properties useful in protein research. It is sensitive to changes in protein structures and to protein redox states, representing a new tool for protein analysis applicable in biomedicine. Electroactivity of nucleic acids was discovered about 50 years ago. Electrochemistry of DNA and RNA is now a booming field because of its potential use in sensors for DNA hybridization and DNA damage. Quite recently it has been shown that electrochemistry can be applied also in polysaccharide analysis. A review with 99 references.

Direct electrochemistry of single-stranded DNA on an ionic liquid modified carbon paste electrode

Electrochemical oxidation of thermally denatured single-stranded DNA (ssDNA) was studied on a room temperature ionic liquid N-butylpyridinium hexafluorophosphate (BPPF 6) modified carbon paste electrode (IL-CPE). A distinct oxidation peak appeared at +0.772 V (vs. SCE) on the IL-CPE after preconcentration of ssDNA at +0.35 V for 160 s in pH 7.0 phosphate buffer solution (PBS), which was attributed to the oxidation of guanine residue on the ssDNA molecular structure. The results showed an apparent negative shift of the oxidation peak potential and a great enhancement of the oxidation peak current on the IL-CPE compared with that of CPE. The electrochemical parameters of ssDNA on the IL-CPE were further calculated. Under the selected conditions, a linear calibration curve for ssDNA detection was obtained in the concentration range from 10.0 to 110.0 μg mL −1 with the detection limit of 1.5 μg mL −1(3σ).

Reversible electrochemistry of DNA on multi-walled carbon nanotube modified electrode

Calf thymus DNA was electrochemically oxidized at a multi-walled carbon nanotube modified electrode. The potentials for DNA oxidation at pH 7.0 were 0.71 and 0.81 V versus SCE, corresponding to the oxidation of guanine and adenine residues, respectively. The initial 6e-oxidation of adenine, observed in the first scan, resulted a quasi-reversible 2e-redox process of the oxidation product in the following scans.

Electrochemical DNA Sensors

AbstractFor Abstract see ChemInform Abstract in Full Text.

Electrochemistry of DNA at Single‐Wall Carbon Nanotubes

AbstractSingle‐wall carbon nanotubes (SWNTs) can be used as an electrochemical probe to study the electrochemical oxidation of DNA, two voltammetric oxidation peaks corresponding to electrochemical oxidation of guanine and adenine residues in DNA could be observed, demonstrating a new potential application of SWNTs in DNA analysis. Compared to other types of electrode materials, the electrochemical response of natural DNA was greatly enhanced at the SWNT‐modified electrode. This method can be used to investigate the interaction of SWNTs with DNA.

Electrochemical DNA sensors.

Electrochemistry-based sensors offer sensitivity, selectivity and low cost for the detection of selected DNA sequences or mutated genes associated with human disease. DNA-based electrochemical sensors exploit a range of different chemistries, but all take advantage of nanoscale interactions between the target in solution, the recognition layer and a solid electrode surface. Numerous approaches to electrochemical detection have been developed, including direct electrochemistry of DNA, electrochemistry at polymer-modified electrodes, electrochemistry of DNA-specific redox reporters, electrochemical amplifications with nanoparticles, and electrochemical devices based on DNA-mediated charge transport chemistry.

Direct electrochemistry of DNA, guanine and adenine at a nanostructured film-modified electrode.

A nanostructured film electrode, a multi-wall carbon nanotubes (MWNT)-modified glassy carbon electrode (GCE), is described for the simultaneous determination of guanine and adenine. The properties of the MWNT-modified GCE were investigated by scanning electron microscopy (SEM) and cyclic voltammetry. The oxidation peak currents of guanine and adenine increased significantly at the MWNT-modified GCE in contrast to those at the bare GCE. The experimental parameters were optimized and a direct electrochemical method for the simultaneous determination of guanine and adenine was proposed. Using the MWNT-modified GCE, a sensitive and direct electrochemical technique for the measurement of native DNA was also developed, and the value of (G+C)/(A+T) of HCl-digested DNA was detected.

Electrochemical DNA Probes

A report on the status of the electrochemical DNA probes for the detection of a DNA sequence for environmental and clinical studies is presented. The literature on the electrochemistry of DNA in the last ten years is reviewed. Results obtained in this laboratory using an electroactive hybridization indicator for constructing an electrochemical DNA probe are reported.