| نویسندگان | مسعود همدانیان,حسینعلی رفیعی پور,سمانه کاتبی کوشالی |
| همایش | The 11th Biennial Electrochemistry Seminar of Iran |
| تاریخ برگزاری همایش | 2014-9-9 |
| محل برگزاری همایش | رشت |
| نوع ارائه | سخنرانی |
| سطح همایش | ملی |
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.