Recombinant Cytochrome P450 Immobilization for Biosensor Applications

Cristina Paternolli, Mirco Antonini, Paola Ghisellini, and Claudio Nicolini*
Nanoworld Institute and Biophysics Division, University of Genova, Corso Europa, 30, 16132 Genova, Italy, and Fondazione Elba, Via delle Testuggini, Roma, Italy
Langmuir, 2004, 20 (26), pp 11706–11712
DOI: 10.1021/la048081q
Publication Date (Web): November 25, 2004
Copyright © 2004 American Chemical Society

Abstract

Abstract Image

As a result of the very attractive pleiotropic properties of the heme-enzymes, three P450 cytochrome isoforms (P4501A2, P4502B4, P450SCC) have been utilized to identify a general optimal procedure to biodevice assembly for sensing a wide range of organic substances. The Langmuir−Blodgett films appears to yield the best stable working conditions as shown by UV−vis spectrophotometry, nanogravimetry, circular dichroism, and electrochemical characterization, to identify the ordered nanostructures of P450 cytochromes optimal for clozapine, styrene, and cholesterol sensing. Only in the presence of low purity grade protein, as in the case of P4501A2, a gel-matrix was needed to warrant the optimal clozapine sensing. By the combination of proper immobilization, transducer and nanostructured mutants of high-grade stable and selective P450-based sensors appear capable to detect the interaction with a wide range of organic substrates such as fatty acids, drugs, and toxic compounds.

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History

  • Published In Issue December 21, 2004
  • Received July 29, 2004
    Revised October 5, 2004

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