Assessing protein oxidation by inorganic nanoparticles with enzyme-linked immunosorbent assay (ELISA)

Authors

  • Wenjie Sun,

    Corresponding author
    1. Department of Chemical and Environmental Engineering, University of Arizona, P.O. Box 210011, Tucson, Arizona; telephone: +1-520-621 6162; fax: +1-520-621-6048
    • Department of Chemical and Environmental Engineering, University of Arizona, P.O. Box 210011, Tucson, Arizona; telephone: +1-520-621 6162; fax: +1-520-621-6048
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  • Antonia Luna-Velasco,

    1. Department of Chemical and Environmental Engineering, University of Arizona, P.O. Box 210011, Tucson, Arizona; telephone: +1-520-621 6162; fax: +1-520-621-6048
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  • Reyes Sierra-Alvarez,

    1. Department of Chemical and Environmental Engineering, University of Arizona, P.O. Box 210011, Tucson, Arizona; telephone: +1-520-621 6162; fax: +1-520-621-6048
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  • Jim A. Field

    1. Department of Chemical and Environmental Engineering, University of Arizona, P.O. Box 210011, Tucson, Arizona; telephone: +1-520-621 6162; fax: +1-520-621-6048
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  • Additional supporting information may be found in the online version of this article.

Abstract

Growth in the nanotechnology industry is leading to increased production of engineered nanoparticles (NPs). This has given rise to concerns about the potential adverse and toxic effects to biological system and the environment. An important mechanism of NP toxicity is oxidative stress caused by the formation of reactive oxygen species (ROS) or via direct oxidation of biomolecules. In this study, a protein oxidation assay was developed as an indicator of biomolecule oxidation by NPs. The oxidation of the protein, bovine serum albumin (BSA) was evaluated with an enzyme-linked immunosorbent assay (ELISA) to measure the protein carbonyl derivatives formed from protein oxidation. The results showed that some NPs such as Cu(0), CuO, Mn2O3, and Fe(0) caused oxidation of BSA; whereas, many of the other NPs tested were not reactive or very slowly reactive with BSA. The mechanisms involved in the oxidation of BSA protein by the reactive NPs could be attributed to the combined effects of ROS-dependent and direct protein oxidation mechanisms. The ELISA assay is a promising method for the assessment of protein oxidation by NPs, which can provide insights on NP toxicity mechanisms. Biotechnol. Bioeng. 2013; 110: 694–701. © 2012 Wiley Periodicals, Inc.

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