ArticleBiopolymers2026
Stepwise LCST-Type Phase Separation in Mixtures of Short-Chain Elastin-Like Peptides With Minimal Structural Differences.
Article in Biopolymers, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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1 citing paper in PubMed.
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4 authors.
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Abstract
Elastin-like peptides (ELPs) comprise repetitive pentapeptide sequences and exhibit liquid-liquid phase separation through lower critical solution temperature-type behavior. Their stimuli-responsive behavior has enabled diverse applications in biomedical and chemical contexts. Although the miscibility and interactions of ELP mixtures have been previously studied, it remains unclear whether mixtures of short-chain ELPs with minimal differences in intrinsic parameters, such as chain length, can exhibit distinct phase behaviors. In this study, we investigated whether synthetic short-chain ELPs differing in length by only one or two repeat units (i.e., 5 or 10 residues) could exhibit independent phase transitions in mixed systems. Turbidity measurements of single- and two-component ELP solutions supported by UPLC-MS analysis revealed stepwise phase transitions upon heating. Our mechanistic analyses revealed that the mixtures undergo a structural transition from polyproline type II helix to β-sheet or β-turn structures. In addition, although the mixtures exhibited stepwise phase separation, our results indicate that heterotypic interactions influenced the sequential phase behavior. These findings reveal that even subtle variations in the ELP chain length and architecture can drive distinct phase separation, providing a rational strategy for designing functional, multicomponent, responsive peptide-based materials.
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