Preservation of the soft protein corona in distinct flow allows identification of weakly bound proteins

Publication date: Available online 8 June 2018
Source:Acta Biomaterialia
Author(s): C. Weber, J. Simon, V. Mailänder, S. Morsbach, K. Landfester
Nanocarriers that are used for targeted drug delivery come in contact with biological liquid and proteins will adsorb to the nanocarriers' surface to form the so called 'protein corona'. The protein corona defines the biological identity and determines the biological response towards the nanocarriers in the body. To make nanomedicine safe and reliable it is required to get a better insight into this protein corona and, therefore, the adsorbed proteins have to be characterized. Currently, centrifugation is the common method to isolate the protein corona for further investigations. However, with this method it is only possible to investigate the strongly bound proteins, also referred to as 'hard protein corona'. Therefore, we want to introduce a new separation technique to separate nanoparticles including the soft protein corona containing also loosely bound proteins for further characterizations. The used separation technique is the asymmetric flow filed-flow fractionation (AF4). We were able to separate the nanoparticles with proteins forming the soft protein corona and were able to show that only the hard protein co rona directly influences the cell uptake behavior.Statement of significanceCurrently, there is an ongoing debate whether only strongly bound proteins (hard corona) or also loosely bound proteins (soft corona) contribute to the biological identity of nanocarriers, because up to now isolation of the soft corona was not possible. Here, asymmetric flow field-flow fractionation was used to isolate nanoparticles with a preserved soft corona from the biological medium. This enabled the characterization of the soft corona composition and to evaluate its influence on cellular uptake. For our system we found that only the strongly bound proteins (hard corona) determined cell internalization. This method can now be used to evaluate the impact of the soft corona further and to characterize nanomaterials that cannot be separated from blood plasma by other means.

Graphical abstract

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