Nanoparticle-Protein Interaction: Demystifying the Correlation Between Protein Corona and Aggregation Phenomena

TL;DR

This study introduces a multi-technique approach combining scattering and microscopy methods to distinguish protein corona formation from nanoparticle aggregation, aiding nanomedicine development.

Contribution

It presents a novel, efficient methodology to differentiate protein corona and various aggregation states in nanoparticle-protein systems.

Findings

Successfully distinguished protein corona from aggregates.

Provided reliable fractal analysis of aggregates.

Demonstrated applicability to biologically relevant samples.

Abstract

Protein corona formation and nanoparticle aggregation have been heavily discussed over the last years since the lack of fine-mapping of these two combined effects has hindered the targeted delivery evolution and the personalized nanomedicine development. We present a multi-technique approach that combines Dynamic Light and Small-Angle X-ray Scattering techniques with cryo-Transmission Electron Microscopy in a given fashion that efficiently distinguishes protein corona from aggregates formation. This methodology was tested using 25-nm model silica nanoparticles incubated with either model proteins or biologically relevant proteomes (such as fetal bovine serum and human plasma) in buffers of low and high ionic strengths to precisely tune particle-to-protein interactions. In this work, we were able to differentiate protein corona, small aggregates formation, and massive aggregation, as well as obtain fractal information of the aggregates reliably and straightforwardly. The strategy presented here can be expanded to other particle-to-protein mixtures and might be employed as a quality control platform for samples that undergo biological tests.