Issue 46, 2017

Arrested and temporarily arrested states in a protein–polymer mixture studied by USAXS and VSANS

Abstract

We investigate the transition of the phase separation kinetics from a complete to an arrested liquid–liquid phase separation (LLPS) in mixtures of bovine γ-globulin with polyethylene glycol (PEG). The solutions feature LLPS with upper critical solution temperature phase behavior. At higher PEG concentrations or low temperatures, non-equilibrium, gel-like states are found. The kinetics is followed during off-critical quenches by ultra-small angle X-ray scattering (USAXS) and very-small angle neutron scattering (VSANS). For shallow quenches a kinetics consistent with classical spinodal decomposition is found, with the characteristic length (ξ) growing with time as ξt1/3. For deep quenches, ξ grows only very slowly with a growth exponent smaller than 0.05 during the observation time, indicating an arrested phase separation. For intermediate quench depths, a novel growth kinetics featuring a three-stage coarsening is observed, with an initial classical coarsening, a subsequent slowdown of the growth, and a later resumption of coarsening approaching again ξt1/3. Samples featuring the three-stage coarsening undergo a temporarily arrested state. We hypothesize that, while intermittent coarsening and collapse might contribute to the temporary nature of the arrested state, migration-coalescence of the minority liquid phase through the majority glassy phase may be the main mechanism underlying this kinetics, which is also consistent with earlier simulation results.

Graphical abstract: Arrested and temporarily arrested states in a protein–polymer mixture studied by USAXS and VSANS

Supplementary files

Article information

Article type
Paper
Submitted
19 Jul 2017
Accepted
05 Nov 2017
First published
06 Nov 2017

Soft Matter, 2017,13, 8756-8765

Arrested and temporarily arrested states in a protein–polymer mixture studied by USAXS and VSANS

S. Da Vela, C. Exner, R. S. Schäufele, J. Möller, Z. Fu, F. Zhang and F. Schreiber, Soft Matter, 2017, 13, 8756 DOI: 10.1039/C7SM01434A

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