Shen Vincent K, Cheung Jason K, Errington Jeffrey R, Truskett Thomas M
Physical and Chemical Properties Division, National Institute of Standards and Technology, Gaithersburg, Maryland, USA.
Biophys J. 2006 Mar 15;90(6):1949-60. doi: 10.1529/biophysj.105.076497. Epub 2005 Dec 30.
We use highly efficient transition-matrix Monte Carlo simulations to determine equilibrium unfolding curves and fluid phase boundaries for solutions of coarse-grained globular proteins. The model we analyze derives the intrinsic stability of the native state and protein-protein interactions from basic information about protein sequence using heteropolymer collapse theory. It predicts that solutions of low hydrophobicity proteins generally exhibit a single liquid phase near their midpoint temperatures for unfolding, while solutions of proteins with high sequence hydrophobicity display the type of temperature-inverted, liquid-liquid transition associated with aggregation processes of proteins and other amphiphilic molecules. The phase transition occurring in solutions of the most hydrophobic protein we study extends below the unfolding curve, creating an immiscibility gap between a dilute, mostly native phase and a concentrated, mostly denatured phase. The results are qualitatively consistent with the solution behavior of hemoglobin (HbA) and its sickle variant (HbS), and they suggest that a liquid-liquid transition resulting in significant protein denaturation should generally be expected on the phase diagram of high-hydrophobicity protein solutions. The concentration fluctuations associated with this transition could be a driving force for the nonnative aggregation that can occur below the midpoint temperature.
我们使用高效的转移矩阵蒙特卡罗模拟来确定粗粒化球状蛋白质溶液的平衡解折叠曲线和液相边界。我们分析的模型利用杂聚物塌缩理论,从有关蛋白质序列的基本信息中得出天然状态的内在稳定性和蛋白质-蛋白质相互作用。它预测,低疏水性蛋白质的溶液在其解折叠中点温度附近通常呈现单一液相,而高序列疏水性蛋白质的溶液则表现出与蛋白质和其他两亲分子聚集过程相关的温度反转的液-液转变类型。我们研究的最疏水蛋白质溶液中发生的相变延伸到解折叠曲线以下,在稀的、主要是天然相和浓的、主要是变性相之间产生了一个不混溶间隙。这些结果在定性上与血红蛋白(HbA)及其镰刀型变体(HbS)的溶液行为一致,并且它们表明,在高疏水性蛋白质溶液的相图上,通常应该预期会出现导致显著蛋白质变性的液-液转变。与这种转变相关的浓度波动可能是在中点温度以下可能发生的非天然聚集的驱动力。