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bioRxiv · 10.64898/2026.02.21.707152

Fine-Tuning α-Synuclein Phase Separation through Sequence-Optimized Peptide Modulators

Ikenoue, T.·Konuma, T.·Ikegami, T.·Suga, H.
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Abstract

Liquid-liquid phase separation (LLPS) of intrinsically disordered proteins underlies the formation of biomolecular condensates that regulate diverse cellular processes, while its dysregulation contributes to protein aggregation and disease. Despite its importance, molecularly defined and target-specific strategies to control LLPS remain limited. Here, we present a systematic framework for designing de novo peptides that induce and modulate LLPS of -synuclein. By integrating deep mutational scanning with peptide screening, we identified sequence features that govern condensate formation and enabled the creation of optimized peptides with high efficiency and specificity. Biophysical analyses revealed that LLPS efficiency is dictated by the interplay of solubility, multivalency, and cooperative interactions, resulting in a distinctive bell-shaped phase diagram. Thermodynamic measurements and imaging-based analyses further demonstrated that condensate stability and material properties can be rationally tuned through peptide optimization. Together, these findings establish generalizable design principles for engineering LLPS modulators in biologically and pathologically relevant protein systems.

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Ikenoue, T., Konuma, T., Ikegami, T., Suga, H.. 2026-02-21. Fine-Tuning α-Synuclein Phase Separation through Sequence-Optimized Peptide Modulators. https://doi.org/10.64898/2026.02.21.707152

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