Solvation Properties in Biomolecular Condensates

In recent years the importance of the aqueous solvent in influencing protein structure, function, and dynamics has been recognized. Coupling of water molecules to the protein surface results in an interfacial region in which water molecules within this region have distinctly different properties than bulk water. However, the structure and dynamics within this interfacial region are still not easy to access experimentally. Terahertz (THz) spectroscopy has been shown to be a powerful tool to investigate solvent dynamics in bulk solutions. Radiation in the THz regime is directly sensitive to the low frequency collective intermolecular hydrogen-bonding vibrations of water (0.3-6 THz or 10-200 cm-1), and thus to any changes in the hydrogen-bonding network. Changes in these sub-picosecond collective motions, such as protein-water interactions, result in changes in the measured THz absorption. Individual hydrations shells of proteins have been shown to contribute largely to structure-function relationships and ultimately modulate the binding properties of proteins. Here the role of solvation dynamics in the liquid-liquid phase separation (LLPS) of the intrinsically disordered protein fused in sarcoma (FUS) is probed. Characterization of the hydrogen bonding network reveals that water solvating hydrophobic groups is stripped away in the membrane-less FUS biomolecular condensates. Additionally, water left inside of the biomolecular condensates is highly constrained, indicative of a population of bound hydration water. These results uncover the vital role of hydration water in LLPS: the entropically favorable release of unfavorable hydration water serves as a driving force for LLPS.