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The Nonequilibrium Phase and Glass Transition Behavior of β-Lactoglobulin

机译:β-乳球蛋白的非平衡相和玻璃化转变行为

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摘要

Concentrated solutions of bovine β-lactoglobulin were studied using osmotic stress and rheological techniques. At pH 6.0 and 8.0, the osmotic pressure was largely independent of NaCl concentration and could be described by a hard sphere equation of state. At pH 5.1, close to the isoelectric point, the osmotic pressure was lower at the lower NaCl concentrations (0 mM, 100 mM) and was fitted by an adhesive hard sphere model. Liquid-liquid phase separation was observed at pH 5.1 at ionic strengths of 13 mM and below. Comparison of the liquid-liquid and literature solid-liquid coexistence curves showed these solutions to be supersaturated and the phase separation to be nonequilibrium in nature. In steady shear, the zero shear viscosity of concentrated solutions at pH 5.1 was observed at shear rates above 50 s−1. With increasing concentration, the solution viscosity showed a progressive increase, a behavior interpreted as the approach to a colloidlike glass transition at ∼60% w/w. In oscillatory shear experiments, the storage modulus crossed the loss modulus at concentrations of 54% w/w, an indication of the approaching glass transition. Comparison of the viscous behavior with predictions from the Krieger-Dougherty equation indicates the hydrodynamic size of the protein decreases with increasing concentration, resulting in a slower approach to the glass transition than a hard sphere system.
机译:使用渗透压和流变技术研究了牛β-乳球蛋白的浓缩溶液。在pH 6.0和8.0时,渗透压在很大程度上与NaCl浓度无关,可以用硬球状态方程描述。在pH 5.1时,接近等电点,在较低的NaCl浓度(0 mM,100 mM)下,渗透压较低,并通过粘性硬球模型拟合。在pH 5.1和13 mM及以下的离子强度下观察到液-液相分离。液-液共存曲线与文献中的固-液共存曲线比较表明,这些溶液过饱和,并且相分离本质上是非平衡的。在稳定剪切下,在高于50 s -1 的剪切速率下,观察到浓溶液在pH 5.1时的零剪切粘度。随着浓度的增加,溶液粘度显示出逐渐增加的行为,这被解释为以约60%w / w的胶态玻璃化转变的方法。在振荡剪切实验中,储能模量在54%w / w的浓度下与损耗模量相交,这表明玻璃化转变即将来临。粘性行为与Krieger-Dougherty方程的预测结果的比较表明,蛋白质的流体动力学尺寸随浓度的增加而减小,导致玻璃化转变的方法比硬球系统慢。

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