Photon correlation spectroscopy is used to study the internal dynamics of self-assembled charged peptide
fibrils. Short neutral and charged polymeric aggregates have diffusive modes due to whole macromolecular
motion. For long semiflexible fibrils the logarithm of the intermediate scattering function follows a q2t3/4
scaling at long times consistent with a Kratky-Porod free energy and preaveraged Oseen hydrodynamics.
Persistence lengths on the order of micrometers are calculated for the peptide fibrils consistent with
estimates from the liquid-crystalline phase behavior. Fibril diameters (5-35 nm) calculated from the
initial decay of the correlation functions are in agreement with transmission electron microscopy
measurements
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