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• W2140909451 abstract "Disruption of amyloid protein aggregates is one of the potential therapies for treatment of neurodegenerative disorders such as prion diseases. Here, for the first time we report that pH‐independent cationic pyridylphenylene dendrimers are able to disrupt amyloid protein aggregates at physiological pH as exemplified by inclusion bodies of ovine prion protein. The results show that exposure of inclusion bodies to the dendrimers leads to its partial disaggregation and release of the nanosize protein–dendrimer complexes. The complexes were characterized by SDS PAGE, DLS, and Western blotting methods. Thioflavin T fluorescence clearly demonstrated a decrease of amyloidogenic capability of the prion protein upon exposure to the dendrimers. The complexes formed are stable and do not show further aggregation." @default.
• W2140909451 created "2016-06-24" @default.
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• W2140909451 date "2015-10-07" @default.
• W2140909451 modified "2023-10-10" @default.
• W2140909451 title "Disruption of Amyloid Prion Protein Aggregates by Cationic Pyridylphenylene Dendrimers" @default.
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• W2140909451 doi "https://doi.org/10.1002/mabi.201500268" @default.
• W2140909451 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/26445143" @default.
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