The dynamics of PEG‐coated nanoparticles in concentrated protein solutions up to the molecular crowding range

Author:

Otto Ferdinand1,Dallari Francesco2,Westermeier Fabian3,Wieland D. C. Florian4,Parak Wolfgang J.15,Lehmkühler Felix35,Schulz Florian1ORCID

Affiliation:

1. Center for Hybrid Nanostructures Universität Hamburg Hamburg Germany

2. Department of Physics and Astronomy “Galileo Galilei” University of Padova Padova Italy

3. Deutsches Elektronen‐Synchrotron DESY Hamburg Germany

4. Institute of Metallic Biomaterials Helmholtz‐Zentrum Hereon Geesthacht Germany

5. The Hamburg Centre for Ultrafast Imaging Hamburg Germany

Abstract

AbstractPolymer‐coated nanoparticles are widely studied in the context of nanomedicine and it is therefore of utmost importance to understand not only how their structure but also how their colloidal dynamics are affected by physiologically relevant conditions. A characteristic feature of the cytosol of cells is the very high concentration of proteins among other matrix components, often termed macromolecular crowding. Here, the structure and colloidal dynamics of poly(ethylene glycol) (PEG)‐coated gold nanoparticles in the presence of bovine serum albumin (BSA) concentrations ranging from 0 to 265 mg/mL are studied with X‐ray photon correlation spectroscopy. For protein–nanoparticle mixtures with high BSA concentrations, comparable to intracellular levels, a significant deviation of the apparent viscosity from expectations for pure BSA solutions is found. The findings strongly indicate that the nanoscopic viscous properties of the dense protein solutions are significantly affected by the nanoparticles. At these high concentrations, the colloidal stability of the samples depends on the molecular weight of the coating PEG–ligand, whereas at lower concentrations no differences are observed.

Funder

Deutsche Forschungsgemeinschaft

European Synchrotron Radiation Facility

Publisher

Wiley

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