Electrochemical measurement of intraprotein and interprotein electron transfer

• Published in: Biophysics (Oxford) Vol. 58; no. 3; pp. 349 - 354
• Main Authors: Shumyantseva, V. V., Bulko, T. V., Lisitsyna, V. B., Urlacher, V. B., Kuzikov, A. V., Suprun, E. V., Archakov, A. I.
• Format: Journal Article
• Language: English
• Published: Boston Springer US 01.05.2013; Springer Nature B.V
• Subjects: Biological and Medical Physics; Biophysics; Electrolytes; Electrons; Measurement errors; Molecular Biophysics; Physics; Physics and Astronomy; Proteins; cytochrome; electrochemistry; electron transfer; cytochrome P450 BM3; electrocatalysis; CYP102A1
• ISSN: 0006-3509; 1555-6654
• DOI: 10.1134/S0006350913030172

Intramolecular and intermolecular direct (unmediated) electron transfer was studied by electrochemical techniques in a flavohemoprotein cytochrome P450 BM3 (CYP102A1 from Bacillius megaterium ) and between cytochromes b 5 and c . P450 BM3 was immobilized on a screen printed graphite electrode modified with a biocompatible nanocomposite material based on didodecyldimethylammonium bromide (DDAB) and gold nanoparticles. Analytical characteristics of SPG/DDAB/Au/P450 BM3 electrodes were studied with cyclic voltammetry and square wave voltammetry. The electron transport chain in P450 BM3 immobilized on the nanostructured electrode is: electrode → FAD → FMN → heme; i.e., electron transfer takes place inside the cytochrome, in evidence of functional interaction between its diflavin and heme domains. The effects of substrate (lauric acid) or inhibitor (metyrapone or imidazole) binding on the electro-chemical parameters of P450 BM3 were assessed. Electrochemical analysis has also demonstrated intermolecular electron transfer between electrode-immobilized and soluble cytochromes properly differing in redox potentials.