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![Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase](/_next/image?url=https%3A%2F%2Fcloudfront.jove.com%2FCDNSource%2Fteasers%2F55858.jpg&w=3840&q=50)
Protein Film Infrared Electrochemistry Demonstrated for Study of H2 Oxidation by a [NiFe] Hydrogenase
Published on: December 4, 2017
Thick-film electrodes for measurement of superoxide and hydrogen peroxide based on direct protein-electrode contacts
Andrey V Krylov1, Moritz Beissenhirtz, Holger Adamzig
1Analytical Biochemistry, Institute of Biochemistry and Biology, Bldg. 25, University of Potsdam, Karl-Liebknecht-Str. 24-25, 14476, Golm, Germany.
Abstract:
Cytochrome c was immobilized on screen-printed thick-film gold electrodes by a self-assembly approach using mixed monolayers of mercaptoundecanoic acid and mercaptoundecanol. Cyclic voltammetry revealed quasi-reversible electrochemical behavior of the covalently fixed protein with a formal potential of +10 mV vs. Ag/AgCl. Polarized at +150 mV vs. Ag/AgCl the electrode was found to be sensitive to superoxide radicals in the range 300-1200 nmol L(-1). Compared with metal needle electrodes sensitivity and reproducibility could be improved and combined with the easiness of preparation. This allows the fabrication of disposable sensors for nanomolar superoxide concentrations. By changing the electrode potential the sensor can be switched from response to superoxide radicals to hydrogen peroxide-another reactive oxygen species. H(2)O(2) sensitivity can be provided in the range 10-1000 micromol L(-1) which makes the electrode suitable for oxidative stress studies.
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