期刊
JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 14, 期 6, 页码 1556-1563出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.2c02697
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Water actively participates in liquid-liquid phase separation (LLPS) by driving and being involved in the process. LLPS is governed by changes in hydration entropy and enthalpy. To tune LLPS for biological and medical applications, a general model is required to quantify thermodynamic driving forces. In this study, we develop such a model based on measured THz features of hydration populations, revealing the thermodynamic changes and providing a rational means to manipulate LLPS.
Water is more than an inert spectator during liquid-liquid phase separation (LLPS), the reversible compartmentalization of protein solutions into a protein-rich and a dilute phase. We show that LLPS is driven by changes in hydration entropy and enthalpy. Tuning LLPS by adjusting experimental parameters, e.g., addition of co-solutes, is a major goal for biological and medical applications. This requires a general model to quantify thermodynamic driving forces. Here, we develop such a model based on the measured amplitudes of characteristic THz-features of two hydration populations: Cavity-wrap water hydrating hydrophobic patches is released during LLPS leading to an increase in entropy. Bound water hydrating hydrophilic patches is retained since it is enthalpically favorable. We introduce a THzphase diagram mapping these spectroscopic/thermodynamic changes. This provides not only a precise understanding of hydrophobic and hydrophilic hydration driving forces as a function of temperature and concentration but also a rational means to tune LLPS.
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