Molecular insights into the effect of alkanediols on FUS liquid-liquid phase separation.

Abstract

Numerous cell biology studies have used high concentrations of 1,6-hexanediol to dissolve membraneless organelles and disordered protein biomolecular condensates. Yet, little is known about how alkanediols effect liquid-liquid phase separation (LLPS), and why certain alkanediol isomers are more effective. Here, we evaluate the effect of various alkanediols on the archetypal phase separating protein FUS. Low-complexity domain and full-length FUS LLPS is decreased varyingly, while LLPS of FUS RGG-RNA condensates is even enhanced by some alkanediols. NMR experiments show that all diols act similarly, correlating atomistic changes with LLPS-preventing effects. Furthermore, we find no evidence for specific residue interactions - the largest perturbations are seen at backbone and glutamine side-chain hydrogen bonding sites, not hydrophobic/aromatic residues. Furthermore, 1,6 hexanediol favors formation of protein-solvent hydrogen bonds and increases FUS local motions. These findings show how alkanediols affect water-disordered protein interactions, underscoring the difficulty in using alkanediol-derivatives to target dissolution of specific membraneless organelles.