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• W3128996851 abstract "Amyloids are broadly investigated protein misfolding products with characteristic β-sheet assemblies that have an important role in neurodegenerative diseases (e.g., Alzheimer’s disease). While they are usually visualized by staining with Thioflavin-T, Congo Red, or other fluorescent markers, it still arouses a controversy over possible staining molecule influence on the amyloid structure or aggregation process. In this work we present, for the first time, the polarization analysis of two-photon excited autofluorescence of amyloids and confirm that polarization dependence of the observed emission can be correlated with the orientation of fibrils. We show the potential of two-photon excited autofluorescence for resolution of molecular organization of fibrils within amyloid superstructures. This label-free method is compatible with two-photon imaging already applied in investigation of neurodegeneration model in mice." @default.
• W3128996851 created "2021-02-15" @default.
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• W3128996851 date "2021-02-01" @default.
• W3128996851 modified "2023-10-03" @default.
• W3128996851 title "Two-Photon Excited Polarization-Dependent Autofluorescence of Amyloids as a Label-Free Method of Fibril Organization Imaging" @default.
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• W3128996851 doi "https://doi.org/10.1021/acs.jpclett.0c03511" @default.
• W3128996851 hasPubMedCentralId "https://www.ncbi.nlm.nih.gov/pmc/articles/7883390" @default.
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• W3128996851 hasPublicationYear "2021" @default.
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