Quantitative super-resolution imaging of pathological aggregates reveals distinct toxicity profiles in different synucleinopathies

Author:

Morten Michael J.12ORCID,Sirvio Liina12,Rupawala Huzefa12,Mee Hayes Emma12,Franco Aitor3ORCID,Radulescu Carola12,Ying Liming4ORCID,Barnes Samuel J.12ORCID,Muga Arturo3ORCID,Ye Yu12ORCID

Affiliation:

1. Department of Brain Sciences, Imperial College London, London W12 0NN, United Kingdom

2. UK Dementia Research Institute at Imperial College London, London W12 0BZ, United Kingdom

3. Instituto Biofisika, University of the Basque Country (Universidad del País Vasco/Euskal Herriko Unibertsitatea), Leioa, 48940 Spain

4. National Heart and Lung Institute, Imperial College London, London W12 0BZ, United Kingdom

Abstract

Protein aggregation is a hallmark of major neurodegenerative disorders. Increasing data suggest that smaller aggregates cause higher toxic response than filamentous aggregates (fibrils). However, the size of small aggregates has challenged their detection within biologically relevant environments. Here, we report approaches to quantitatively super-resolve aggregates in live cells and ex vivo brain tissues. We show that Amytracker 630 (AT630), a commercial aggregate-activated fluorophore, has outstanding photophysical properties that enable super-resolution imaging of α-synuclein, tau, and amyloid-β aggregates, achieving ∼4 nm precision. Applying AT630 to App NL-G-F mouse brain tissues or aggregates extracted from a Parkinson’s disease donor, we demonstrate excellent agreement with antibodies specific for amyloid-β or α-synuclein, respectively, confirming the specificity of AT630. Subsequently, we use AT630 to reveal a linear relationship between α-synuclein aggregate size and cellular toxicity and discovered that aggregates smaller than 450 ± 60 nm (aggregate 450nm ) readily penetrated the plasma membrane. We determine aggregate 450nm concentrations in six Parkinson’s disease and dementia with Lewy bodies donor samples and show that aggregates in different synucleinopathies demonstrate distinct potency in toxicity. We further show that cell-penetrating aggregates are surrounded by proteasomes, which assemble into foci to gradually process aggregates. Our results suggest that the plasma membrane effectively filters out fibrils but is vulnerable to penetration by aggregates of 450 ± 60 nm. Together, our findings present an exciting strategy to determine specificity of aggregate toxicity within heterogeneous samples. Our approach to quantitatively measure these toxic aggregates in biological environments opens possibilities to molecular examinations of disease mechanisms under physiological conditions.

Funder

UKRI

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

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