Mechanism of silica-lysozyme composite formation unravelled by in situ fast SAXS

TL;DR

This study uses in situ fast SAXS to elucidate the aggregation mechanisms and structural changes during silica-lysozyme composite formation in aqueous solutions, revealing how size matching influences interactions.

Contribution

It introduces a novel scattering model and provides real-time insights into the structural deformation and aggregation mechanisms of silica-lysozyme composites.

Findings

Size matching influences silica-lysozyme interactions

Structural deformation of lysozyme during aggregation

Real-time observation of composite formation mechanisms

Abstract

A quantitative understanding of aggregation mechanisms leading to the formation of inorganic nanoparticles (NPs) and protein composites in aqueous media is of paramount interest for colloid chemistry. In particular, the interactions between silica (SiO2) NPs and lysozyme (LZM) have attracted attention, because LZM is well-known to adsorb strongly to silica NPs, while at the same time preserving its enzymatic activity. The inherent nature of the aggregation processes leading to NP-LZM composites involves structural changes at length-scales from few to hundreds of nanometres but also time scales << 1 second. To unravel these we used in situ synchrotron-based small-angle X-ray scattering (SAXS) and followed the subtle interparticle interactions in solution at a time resolution of 50 ms/frame (20 fps). We show that if the size of silica NPs (~5 nm diameter) is matched by the dimensions of LZM, the evolving scattering patterns contain a unique structure factor contribution originating from the presence of LZM. We developed a scattering model and applied it to analyse this structure function, which allowed us to extract structural information on the deformation of lysozyme molecules during aggregation, as well as to derive the mechanisms of composite formation.