Department of Chemical and Biomolecular Engineering, North Carolina State University , Raleigh, North Carolina 27606, United States.
Department of Chemical Engineering, Imperial College London , London SW7 2AZ, United Kingdom.
Langmuir. 2017 Oct 24;33(42):11733-11745. doi: 10.1021/acs.langmuir.7b02249. Epub 2017 Sep 21.
The statistical associating fluid theory for potentials of variable range (SAFT-VR) is used to predict the fluid phase behavior of elastin-like polypeptide (ELP) sequences in aqueous solution with special focus on the loci of lower critical solution temperatures (LCSTs). A SAFT-VR model for these solutions is developed following a coarse-graining approach combining information from atomistic simulations and from previous SAFT models for previously reported relevant systems. Constant-pressure temperature-composition phase diagrams are determined for solutions of (VPGVG) sequences + water with n = 1 to 300. The SAFT-VR equation of state lends itself to the straightforward calculation of phase boundaries so that complete fluid-phase equilibria can be calculated efficiently. A broad range of thermodynamic conditions of temperature and pressure are considered, and regions of vapor-liquid and liquid-liquid coexistence, including LCSTs, are found. The calculated phase boundaries at low concentrations match those measured experimentally. The temperature-composition phase diagrams of the aqueous ELP solutions at low pressure (0.1 MPa) are similar to those of types V and VI phase behavior in the classification of Scott and van Konynenburg. An analysis of the high-pressure phase behavior confirms, however, that a closed-loop liquid-liquid immiscibility region, separate from the gas-liquid envelope, is present for aqueous solutions of (VPGVG); such a phase diagram is typical of type VI phase behavior. ELPs with shorter lengths exhibit both liquid-liquid and gas-liquid regions, both of which become less extensive as the chain length of the ELP is decreased. The strength of the hydrogen-bonding interaction is also found to affect the phase diagram of the (VPGVG) system in that the liquid-liquid and gas-liquid regions expand as the hydrogen-bonding strength is decreased and shrink as it is increased. The LCSTs of the mixtures are seen to decrease as the ELP chain length is increased.
变程势统计缔合流体理论(SAFT-VR)用于预测弹性蛋白样多肽(ELP)序列在水溶液中的流体相行为,特别关注下临界溶液温度(LCST)的位置。根据一种粗粒化方法,结合来自原子模拟和先前针对相关系统的 SAFT 模型的信息,为这些溶液开发了一个 SAFT-VR 模型。对于(VPGVG)序列+水的 n = 1 到 300 的溶液,确定了等压温度组成相图。SAFT-VR 状态方程易于直接计算相边界,因此可以有效地计算完整的流体相平衡。考虑了广泛的温度和压力热力学条件,并找到了汽液和液液共存的区域,包括 LCST。在低浓度下计算出的相边界与实验测量值相匹配。在低压力(0.1 MPa)下,水溶液 ELP 溶液的温度组成相图类似于 Scott 和 van Konynenburg 分类中的类型 V 和 VI 相行为。对高压相行为的分析证实,对于(VPGVG)的水溶液,存在与气液包络线分开的闭路液-液不混溶性区域,这种相图是典型的类型 VI 相行为。较短长度的 ELP 表现出液-液和气-液区域,随着 ELP 链长的减小,这两个区域都变得不那么广泛。还发现氢键相互作用的强度也会影响(VPGVG)系统的相图,即随着氢键强度的降低,液-液和气-液区域扩大,随着氢键强度的增加而收缩。随着 ELP 链长的增加,混合物的 LCST 降低。