Direct electrochemistry of cytochrome c on TiO۲/Au nanocomposite modified electrode

نویسندگانمسعود همدانیان,حسینعلی رفیعی پور,سمانه کاتبی کوشالی
همایشThe 11th Biennial Electrochemistry Seminar of Iran
تاریخ برگزاری همایش۲۰۱۴-۹-۹
محل برگزاری همایشرشت
نوع ارائهسخنرانی
سطح همایشملی

چکیده مقاله

Direct electrochemistry between redox proteins and electrode surface has been extensively studied because of its potential application in the investigation of biomolecules [1]. Cytochrome c (Cyt. c) is an excellent model for studying the electron transfer of typical metalloproteins from a structure point of view. Due to the difficulty of direct electron transfer between Cyt c and a bare electrode, some modified electrodes were used as a tool to investigate the direct electrochemical property. The modifiers of these modified electrodes are organic [2], or inorganic [3] compounds.In the present study, we explored the ability of TiO2/Au nanocompositeto act as modifier to realize the direct electron transfer (DET) of Cyt c. The investigation on titanium dioxide (TiO2), a kind of inorganic porous material with unique construction, high surface area and high chemical stability, had shown that it could be used as an electrode material to promote electron-transfer reactions of protein. We investigated the formation of a hybrid biointerface consisting of gold-doped titanium dioxide (TiO2/Au) film and cytochrome c (Cyt c) on indium tin oxide (ITO) electrodes. The TiO2/Au film provided a good microenvironment for the immobilization of biomolecules enhanced the surface coverage of protein, had large surface-to-volume ratio, and high stability. Cyclic voltammetry (CV) was performed to evaluate electrochemical properties of the as prepared interface. The ITO/TiO2/Au /Cyt c electrode display a pair of well-defined redox peak ( 0.06 V and 0.02 V) at pH 7.0 in phosphate buffer solution. These nanoparticles inhibit the adsorption of Cyt c onto bare electrode and act as a bridge of electron transfer between protein and electrode.