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Gelation Dynamics upon Pressure-Induced Liquid-Liquid Phase Separation in a Water-Lysozyme Solution

Moron, M. (author)
Al-Masoodi, A. (author)
Lovato, C. (author)
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Reiser, Mario (author)
Stockholms universitet,Fysikum
Randolph, L. (author)
Surmeier, G. (author)
Bolle, J. (author)
Westermeier, F. (author)
Sprung, M. (author)
Winter, R. (author)
Paulus, M. (author)
Gutt, C. (author)
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 (creator_code:org_t)
2022-05-20
2022
English.
In: Journal of Physical Chemistry B. - : American Chemical Society (ACS). - 1520-6106 .- 1520-5207. ; 126:22, s. 4160-4167
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • 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 g2 functions display a two-step decay with a gradually increasing nonergodicity parameter typical for gelation. We observe fast superdiffusive (γ ≥ 3/2) and slow subdiffusive (γ < 0.6) motion associated with fast viscoelastic fluctuations of the network and a slow viscous coarsening process, respectively. The dynamics age linearly with time τ ∝ tw, and we observe the onset of viscoelastic relaxation for deeper quenches. Our results suggest that the protein solution gels upon reaching the phase boundary.

Subject headings

NATURVETENSKAP  -- Kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences (hsv//eng)

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