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Fig. 4 | Alzheimer's Research & Therapy

Fig. 4

From: A novel D-amino acid peptide with therapeutic potential (ISAD1) inhibits aggregation of neurotoxic disease-relevant mutant Tau and prevents Tau toxicity in vitro

Fig. 4

ISAD1 and ISAD1rev inhibit the aggregation of TauFL and TauRDΔK. A Fibrillization curves of TauFL in the presence of different concentrations of the peptide ISAD1 over a period of 24 h. The assay was performed using 5 μM TauFL with 1.25 μM heparin (H16K) and 10 μM ThT in HEPES buffer. ISAD1 was added in concentrations of 0.1 nM to 200 μM. B Dose-response curve of TauFL fibrillization process in the presence of ISAD1 and ISAD1rev (0.1 nM–200 μM). C 10 μM TauRDΔK in BES buffer was incubated with 2.5 μM heparin and 20 μM ThS to monitor fibrillization. D Dose-response curve of TauRDΔK in the presence of ISAD1 and ISAD1rev. The relative fluorescence of a buffer sample was subtracted. Fluorescence was measured at 520 nm in relative units (mean ± standard deviations of results, three replicates per run). The fluorescence of TauFL, TauRDΔK was set as 100% and the values and standard deviations of the other incubations are given as percentages of this maximum value. The data represent the mean values ± SD with n = 3 determinations

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