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Analytical Biochemistry
Volume 375, Issue 2, 15 April 2008, Pages 209-216
 
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doi:10.1016/j.ab.2007.12.001    How to Cite or Link Using DOI (Opens New Window)
Copyright © 2007 Elsevier Inc. All rights reserved.

Electrochemistry of cytochrome P450 enzyme on nanoparticle-containing membrane-coated electrode and its applications for drug sensing

Songqin Liua, Corresponding Author Contact Information, E-mail The Corresponding Author, Lei Pengb, Xiaodi Yangb, Corresponding Author Contact Information, E-mail The Corresponding Author, Yafeng Wua and Lin Hec

aState Key Laboratory of Bioelectronics and Jiangsu Provincial Key Laboratory of Biomaterials and Biodevices, School of Chemistry and Chemical Engineering, Southeast University, Nanjing 210096, People’s Republic of China bJiangsu Key Laboratory of Biofunctional Materials, College of Chemistry and Environmental Science, Nanjing Normal University, Nanjing 210097, People’s Republic of China cDepartment of Chemistry, North Carolina State University, Raleigh, NC 27695, USA

Received 1 November 2007. 
Available online 7 December 2007.

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Abstract

In the current study, we describe an improved system to study the two-electron delivery reaction pathway of cytochrome P450, family 2, subfamily B, polypeptide 6 (CYP2B6) in vitro. In particular, a biocompatible film containing colloidal gold nanoparticles and chitosan was used to encapsulate CYP2B6 on an electrode. The electrocatalytic behaviors of CYP2B6 toward common drugs in the absence of NADHP–cytochrome P450 reductase as electron donor were studied. In an anaerobic solution, direct and reversible electron transfer between the electroactive heme center of CYP2B6 and the electrode was observed with a formal potential of –0.454 ± 0.006 V at pH 7.4. In an air-saturated solution, an increase in the bioelectrocatalytic reduction current was observed after drug addition. The bioelectrocatalytic products were analyzed using high-performance liquid chromatography (HPLC) and electrospray ionization–mass spectrometry (ESI–MS). Both results confirmed that C-hydroxylation and heteroatom release were the main pathways for CYP2B6-mediated drug oxidation, similar to what occurred in vivo. The use of immobilized proteins in nanoparticle-containing films in drug biosensing was also demonstrated.

Keywords: Cytochrome P450 2B6; Colloidal gold nanoparticles; Bupropion; Bioelectrocatalysis; Drug metabolism

Article Outline

Materials and methods
Materials
Modification of the electrodes
Electrochemical measurements
Spectroscopic analysis
High-performance liquid chromatographic and electrospray ionization mass spectrometric analysis
Results and discussion
Direct electrochemistry of CYP2B6/Au–chitosan electrode
Electrocatalysis of CYP2B6/Au–chitosan/GCE to oxygen
Electrocatalysis of CYP2B6/Au–chitosan/GCE to the commonly used drugs
Conclusions
Acknowledgements
Appendix A. Supplementary data
References







Analytical Biochemistry
Volume 375, Issue 2, 15 April 2008, Pages 209-216
 
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