Issue 6, 2022

Amyloid fibrils in superstructures – local ordering revealed by polarization analysis of two-photon excited autofluorescence

Abstract

Protein misfolding products – amyloids – tend to form distinct fibrillar structures of the characteristic fold for a given neurodegenerative disease or pathology. Moreover, amyloids (also in the intermediate or distorted state) can act as secondary nuclei for de novo fibrillation. Such secondary nucleation amplifies plaque development correlated with various diseases. Therefore, a versatile and non-destructive method of detection and differentiation between distinct fibrillar structures is of great importance. Amyloids exhibit unique optical properties, i.e. green-blue autofluorescence, which can also be induced by two-photon excitation. Herein, we use this label-free technique to resolve local fibrillar ordering in amyloid superstructures – spherulites. With polarization-dependent two-photon excited amyloid autofluorescence, we resolved fibrillar orientation in the spherulite corona and discussed the presence of amorphous aggregates, distorted fibrils or amyloid intermediate species within the spherulite core. Our polarization sensitive two-photon microscopy investigations are supported by TEM imaging and provide a promising tool for the detection and differentiation between well-developed amyloid fibrils and amorphous/distorted structures present at different stages of the formation of amyloid superstructures and plaques.

Graphical abstract: Amyloid fibrils in superstructures – local ordering revealed by polarization analysis of two-photon excited autofluorescence

Supplementary files

Article information

Article type
Paper
Submitted
19 Nov 2021
Accepted
28 Jan 2022
First published
28 Jan 2022
This article is Open Access
Creative Commons BY license

Biomater. Sci., 2022,10, 1554-1561

Amyloid fibrils in superstructures – local ordering revealed by polarization analysis of two-photon excited autofluorescence

P. Obstarczyk, M. Lipok, A. Żak, P. Cwynar and J. Olesiak-Bańska, Biomater. Sci., 2022, 10, 1554 DOI: 10.1039/D1BM01768C

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