Crowding-induced phase separation and solidification by co-condensation of PEG in NPM1-rRNA condensates

Abstract

ABSTRACTThe crowdedness of the cell calls for adequate intracellular organization. Biomolecular condensates, formed by liquid-liquid phase separation of intrinsically disordered proteins and nucleic acids, are important organizers of cellular fluids. To underpin the molecular mechanisms of protein condensation, cell-free studies are often used where the role of crowding is not investigated in detail. Here, we investigate the effects of macromolecular crowding on the formation and material properties of a model heterotypic biomolecular condensate, consisting of nucleophosmin (NPM1) and ribosomal RNA (rRNA). We studied the effect of the macromolecular crowding agent PEG, which is often considered an inert crowding agent. We observed that PEG could induce both homotypic and heterotypic phase separation of NPM1 and NPM1-rRNA, respectively. Crowding increases the condensed concentration of NPM1 and decreases its equilibrium dilute phase concentration, while no significant change in the concentration of rRNA in the dilute phase was observed. Interestingly, the crowder itself is concentrated in the condensates, suggesting that co-condensation rather than excluded volume interactions underlie the enhanced phase separation by PEG. Fluorescence recovery after photobleaching (FRAP) measurements indicated that both NPM1 and rRNA become immobile at high PEG concentrations, indicative of a liquid-to-gel transition. Together, these results shed new light onto the role of synthetic crowding agents in phase separation, and demonstrate that condensate properties determined in vitro depend strongly on the addition of crowding agents.STATEMENT OF SIGNIFICANCELiquid-liquid phase separation of proteins and nucleic acids leads to the formation of biomolecular condensates. To mimic biomolecular condensates in vitro, polymeric crowding agents, such as PEG, are often added. Such crowding agents are considered to make in vitro solutions more physiologically relevant, by mimicking the high cellular macromolecule concentrations. However, these crowding agents are commonly selected for their commercial availability and solubility in water, and their influence on phase separation and the physicochemical properties of condensates are seldom studied. Here we use biophysical methods to show that PEG induces phase separation of a model condensate through co-condensation rather than volume exclusion. As a consequence, crowding changes the partitioning, concentrations and viscoelastic properties of the condensates significantly, which sheds new light onto studies aimed at quantifying the material properties of biomolecular condensates.