Gelation dynamics upon pressure-induced liquid-liquid phase separation in a water-lysozyme solution

Employing X-ray photon correlation spectroscopy we measure the kinetics and dynamics of a pressure-induced liquid-liquid phase separation (LLPS) in a water-lysozyme solution. Scattering invariants and kinetic information provide evidence that the system reaches the phase boundary upon pressure-induc...

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Hauptverfasser: Moron, M, Al-Masoodi, A, Lovato, C, Reiser, M, Randolph, L, Surmeier, G, Bolle, J, Westermeier, F, Sprung, M, Winter, R, Paulus, M, Gutt, C
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creator Moron, M
Al-Masoodi, A
Lovato, C
Reiser, M
Randolph, L
Surmeier, G
Bolle, J
Westermeier, F
Sprung, M
Winter, R
Paulus, M
Gutt, C
description Employing X-ray photon correlation spectroscopy we measure the kinetics and dynamics of a pressure-induced liquid-liquid phase separation (LLPS) in a water-lysozyme solution. Scattering invariants and kinetic information provide evidence that the system reaches the phase boundary upon pressure-induced LLPS with no sign of arrest. The coarsening slows down with increasing quench depths. The $g_2$-functions display a two-step decay with a gradually increasing non-ergodicity parameter typical for gelation. We observe fast superdiffusive ($\gamma \geq 3/2$) and slow subdiffusive ($\gamma < 0.6$) motion associated with fast viscoelastic fluctuations of the network and a slow viscous coarsening process, respectively. The dynamics age linear with time $\tau \propto t_\mathrm{w}$ and we observe the onset of viscoelastic relaxation for deeper quenches. Our results suggest that the protein solution gels upon reaching the phase boundary.
doi_str_mv 10.48550/arxiv.2107.05026
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title Gelation dynamics upon pressure-induced liquid-liquid phase separation in a water-lysozyme solution
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