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. 2023 Sep 14;16(1):89–97. doi: 10.1038/s41557-023-01321-y

Fig. 1. Design and assembly of de novo polypeptides for biomolecular condensation.

Fig. 1

a, Cartoon for membraneless-organelle formation in cells, that is, protein condensation leading to the formation of de-mixed droplets. b, Protein solutions can form a single phase, or phase-separated systems including condensates, aggregates and gels. c, HERD design strategy for phase separation by concatenation of de novo CCs. d, Helical wheels of the heptad (seven-residue) repeats for trimeric (left) and tetrameric (right) CCs with hydrophobic interface residues in blue and solvent-exposed residues in black. eg, Weakening of PPIs by truncating the helical CC lengths (e), disrupting packing in the hydrophobic core through Ile/Leu (left) to Ala (right) mutations to the a position in the abcdefg heptad repeat (f) and reducing helical propensity by replacing surface residues to those with a low helical propensities (g).