Shiv Rekhi, Jeetain Mittal
High Resolution Image Download MS PowerPoint Slide Biomolecular condensates create distinct solvation environments in which the ionization equilibria of amino acid side chains may differ markedly from those in a bulk aqueous solution. Here, we use all-atom continuous constant pH molecular dynamics simulations to investigate the changes to the p K a values of titratable residues between the coexisting phases of biomolecular condensates. We found that protonated states are favored in the condensate, resulting in the stabilization of charged forms of cationic residues and neutral forms of anionic residues. The effect is consistent across condensates formed by five peptide sequences, suggesting that the preference for protonated states is a general feature of the condensate microenvironment. These results highlight that differences in solvation environments between coexisting phases are key determinants of charge regulation in phase-separating proteins.