Coherent X-rays reveal anomalous molecular diffusion and cage effects in crowded protein solutions
Understanding protein motion within the cell is crucial for predicting reaction rates and macromolecular transport in the cytoplasm. A key question is how crowded environments affect protein dynamics through hydrodynamic and direct interactions at molecular length scales. Using megahertz X-ray Photo...
Saved in:
Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Format | Journal Article |
Language | English |
Published |
11.10.2024
|
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | Understanding protein motion within the cell is crucial for predicting
reaction rates and macromolecular transport in the cytoplasm. A key question is
how crowded environments affect protein dynamics through hydrodynamic and
direct interactions at molecular length scales. Using megahertz X-ray Photon
Correlation Spectroscopy (MHz-XPCS) at the European X-ray Free Electron Laser
(EuXFEL), we investigate ferritin diffusion at microsecond time scales. Our
results reveal anomalous diffusion, indicated by the non-exponential decay of
the intensity autocorrelation function $g_2(q,t)$ at high concentrations. This
behavior is consistent with the presence of cage-trapping in between the short-
and long-time protein diffusion regimes. Modeling with the
$\delta\gamma$-theory of hydrodynamically interacting colloidal spheres
successfully reproduces the experimental data by including a scaling factor
linked to the protein direct interactions. These findings offer new insights
into the complex molecular motion in crowded protein solutions, with potential
applications for optimizing ferritin-based drug delivery, where protein
diffusion is the rate-limiting step. |
---|---|
DOI: | 10.48550/arxiv.2410.08873 |