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Issue 34, 2019
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Maghemite nanoparticles stabilize the protein corona formed with transferrin presenting different iron-saturation levels

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Abstract

Magnetic nanoparticles are ideal candidates for biomedical applications given their potential use in magnetic resonance imaging, magnetic hyperthermia and targeted drug delivery. Understanding protein–nanoparticle interactions in the blood stream is of major importance due to their potential risks, especially immunogenicity (i.e. the ability to induce an immune response). Here, we report on the interaction of superparamagnetic maghemite (γ-Fe2O3) nanoparticles with human blood plasma protein transferrin presenting different iron-saturation levels: partially iron-saturated (i.e. transferrin) and iron-free transferrin (i.e. apotransferrin). The nanoparticle–protein interaction and the protein corona formation were studied using biophysical and chemical approaches based on dynamic light scattering, gel electrophoresis, circular dichroism spectroscopy and differential scanning fluorimetry. We found that iron content governs the protein corona formation and induces a strong effect on the thermal stability of the bound protein. Our results demonstrate a stabilizing effect of the nanoparticles with a change of the unfolding position of approximately 10 °C towards higher temperatures for transferrin. Our study may be relevant for the further development of magnetic nanoparticles as diagnostic and therapeutic tools.

Graphical abstract: Maghemite nanoparticles stabilize the protein corona formed with transferrin presenting different iron-saturation levels

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Publication details

The article was received on 11 Jun 2019, accepted on 29 Jul 2019 and first published on 29 Jul 2019


Article type: Paper
DOI: 10.1039/C9NR04967C
Nanoscale, 2019,11, 16063-16070

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    Maghemite nanoparticles stabilize the protein corona formed with transferrin presenting different iron-saturation levels

    U. Martens, D. Böttcher, D. Talbot, U. Bornscheuer, A. Abou-Hassan and M. Delcea, Nanoscale, 2019, 11, 16063
    DOI: 10.1039/C9NR04967C

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