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通过 USAXS 和 VSANS 研究的蛋白质-聚合物混合物中的被捕获和暂时被捕获状态。

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

机构信息

Institut für Angewandte Physik, Universität Tübingen, Auf der Morgenstelle 10, 72076 Tübingen, Germany.

出版信息

Soft Matter. 2017 Nov 29;13(46):8756-8765. doi: 10.1039/c7sm01434a.

DOI:10.1039/c7sm01434a
PMID:29130090
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 ξ ∼ t. 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 ξ ∼ t. 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.

摘要

我们研究了牛γ-球蛋白与聚乙二醇(PEG)混合物中从完全到被阻止的液-液相分离(LLPS)的相分离动力学转变。这些溶液具有上临界溶液温度相行为的 LLPS。在较高的 PEG 浓度或低温下,会发现非平衡的凝胶状状态。通过超小角 X 射线散射(USAXS)和甚小角中子散射(VSANS)在非临界淬火过程中跟踪动力学。对于较浅的淬火,发现动力学与经典的旋节线分解一致,特征长度(ξ)随时间增长,ξ∼t。对于深淬火,ξ 的增长非常缓慢,在观察时间内生长指数小于 0.05,表明相分离被阻止。对于中间淬火深度,观察到具有三个阶段粗化的新型生长动力学,具有初始经典粗化、随后生长减速、以及随后再次接近 ξ∼t 的恢复粗化。具有三个阶段粗化的样品经历了暂时被阻止的状态。我们假设,虽然间歇式粗化和崩溃可能导致被阻止状态的暂时性,但少数液相通过多数玻璃相的迁移-合并可能是这种动力学的主要机制,这也与早期的模拟结果一致。

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