Randomized trial investigates hydrogen-bond dynamics influenced by peptide length in biocondensates, suggesting molecular design implications.
Biomolecular condensates create distinct chemical environments that modulate molecular interactions and solvent organization, yet how the peptide length shapes the local hydrogen-bonding landscape remains unclear. Here, poly-l-arginine (poly-R) with adenosine monophosphate (AMP) is used to isolate chain-length effects on local hydrogen-bond environments. Four poly-R lengths (10-, 30-, 50-, and 100-mer) were characterized using FTIR and ultrafast two-dimensional IR (2D IR) spectroscopy. Line shapes indicate invariant backbone conformations, whereas picosecond dynamics exhibit strong length dependence. In dilute solution, correlation lifetimes increase with peptide length, consistent with hindered solvent rearrangement around compact polyelectrolyte chains. In the condensed phase, dynamics become nonlinear, with longer chains exhibiting pronounced slowing consistent with enhanced multivalency, increased network connectivity, and partial dynamic arrest. Simulations provide an atomistic picture of this slowdown. Together, these results show that the chain length lowers the entropic cost of association and promotes network formation, determining local chemical environments in biocondensates.
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Sheehan et al. (2026) studied this question.
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