## Abstract A novel nanohybrid material, constructed by gold nanoparticles (GNPs) and multiwalled carbon nanotubes (MWNTs), was designed for immobilization and biosensing of myoglobin (Mb). Morphology of the nanohybrid film was characterized by SEM. UVβvis spectroscopy demonstrated that Mb on the c
Electrocatalysis via Direct Electrochemistry of Myoglobin Immobilized on Colloidal Gold Nanoparticles
β Scribed by Songqin Liu; Huangxian Ju
- Publisher
- John Wiley and Sons
- Year
- 2003
- Tongue
- English
- Weight
- 147 KB
- Volume
- 15
- Category
- Article
- ISSN
- 1040-0397
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β¦ Synopsis
Abstract
The direct electron transfer between immobilized myoglobin (Mb) and colloidal gold modified carbon paste electrode was studied. The Mb immobilized on the colloidal gold nanoparticles displayed a pair of redox peaks in 0.1 M pHβ 7.0 PBS with a formal potential of β(0.108 Β± 0.002) V (vs. NHE). The response showed a surfaceβcontrolled electrode process with an electron transfer rate constant of (26.7 Β± 3.7) s ^β1^ at scan rates from 10 to 100β mV s^β1^ and a diffusionβcontrolled process involving the diffusion of proton at scan rates more than 100β mV s^β1^. The immobilized Mb maintained its activity and could electrocatalyze the reduction of both hydrogen peroxide and nitrite. Thus, the novel renewable reagentless sensors for hydrogen peroxide and nitrite were developed, respectively. The activity of Mb with respect to the pseudo peroxidase with a K~M~^app^ value of 0.65β mM could respond linearly to hydrogen peroxide concentration from 4.6 to 28β ΞΌM. The sensor exhibited a fast amperometric response to NO~2~^β^ reduction and reached 93% of steadyβstate current within 5β s. The linear range for NO~2~^β^ determination was from 8.0 to 112β ΞΌM with a detection limit of 0.7β ΞΌM at 3__Ο__.
π SIMILAR VOLUMES
Direct electron transfer of immobilized horseradish peroxidase on gold colloid and its application as a biosensor were investigated by using electrochemical methods. The Au colloids were associated with a cysteamine monolayer on the gold electrode surface. A pair of redox peaks attributed to the dir