Fakultät Physik/DELTA, TU Dortmund, 44221 Dortmund, Germany.
Department Physik, Naturwissenschaftlich-Technische Fakultät, Universität Siegen, 57068 Siegen, Germany.
J Phys Chem B. 2022 Jun 9;126(22):4160-4167. doi: 10.1021/acs.jpcb.2c01947. Epub 2022 May 20.
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 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 ∝ , and we observe the onset of viscoelastic relaxation for deeper quenches. Our results suggest that the protein solution gels upon reaching the phase boundary.
采用 X 射线光子相关光谱法,我们测量了水溶溶菌酶溶液中压力诱导的液-液相分离(LLPS)的动力学和动态特性。散射不变量和动力学信息表明,系统在压力诱导的 LLPS 达到相边界,没有停滞的迹象。随着淬火深度的增加,粗化过程减缓。 函数显示出两步衰减,非遍历参数逐渐增加,这是凝胶化的典型特征。我们观察到与网络的快速粘弹性波动相关的快超扩散(γ≥3/2)和慢亚扩散(γ<0.6)运动,以及与慢粘性粗化过程相关的慢亚扩散运动。动力学年龄与时间τ∝线性相关,我们观察到较深淬火时粘弹性松弛的开始。我们的结果表明,蛋白质溶液在达到相边界时会凝胶化。