Novel tools to quantify total, phospho-Ser129 and aggregated alpha-synuclein in the mouse brain

Assays for quantifying aggregated and phosphorylated (S129) human α-synuclein protein are widely used to evaluate pathological burden in patients suffering from synucleinopathy disorders. Many of these assays, however, do not cross-react with mouse α-synuclein or exhibit poor sensitivity for this target, which is problematic considering the preponderance of mouse models at the forefront of pre-clinical α-synuclein research. In this project, we addressed this unmet need by reformulating two existing AlphaLISA<sup>®</sup> SureFire<sup>®</sup> Ultra™ total and pS129 α-synuclein assay kits to yield robust and ultrasensitive (LLoQ ≤ 0.5 pg/mL) quantification of mouse and human wild-type and pS129 α-synuclein protein. We then employed these assays, together with the BioLegend α-synuclein aggregate ELISA, to assess α-synuclein S129 phosphorylation and aggregation in different mouse brain tissue preparations. Overall, we highlight the compatibility of these new immunoassays with rodent models and demonstrate their potential to advance knowledge surrounding α-synuclein phosphorylation and aggregation in synucleinopathies.

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Publication Details

Journal
npj Parkinson s Disease
Published
2024-11-08
DOI
https://doi.org/10.1038/s41531-024-00830-y
Citations
5
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
1.85

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article

Novel tools to quantify total, phospho-Ser129 and aggregated alpha-synuclein in the mouse brain

Nicolas Dzamko, Louise Cottle, Nanna Møller Jensen, Alejandra Rangel et al.
5 citations
npj Parkinson s Disease
Parkinson's Disease Mechanisms and Treatments
1.85
article

Novel tools to quantify total, phospho-Ser129 and aggregated alpha-synuclein in the mouse brain

Nicolas Dzamko, Louise Cottle, Nanna Møller Jensen, Alejandra Rangel, Hjalte Gram, Poul Henning Jensen, Courtney Jade Wright, Asheeta Prasad, Deniz Kirik, Benjamin G. Trist
article en
5 citations

Abstract

Assays for quantifying aggregated and phosphorylated (S129) human α-synuclein protein are widely used to evaluate pathological burden in patients suffering from synucleinopathy disorders. Many of these assays, however, do not cross-react with mouse α-synuclein or exhibit poor sensitivity for this target, which is problematic considering the preponderance of mouse models at the forefront of pre-clinical α-synuclein research. In this project, we addressed this unmet need by reformulating two existing AlphaLISA<sup>®</sup> SureFire<sup>®</sup> Ultra™ total and pS129 α-synuclein assay kits to yield robust and ultrasensitive (LLoQ ≤ 0.5 pg/mL) quantification of mouse and human wild-type and pS129 α-synuclein protein. We then employed these assays, together with the BioLegend α-synuclein aggregate ELISA, to assess α-synuclein S129 phosphorylation and aggregation in different mouse brain tissue preparations. Overall, we highlight the compatibility of these new immunoassays with rodent models and demonstrate their potential to advance knowledge surrounding α-synuclein phosphorylation and aggregation in synucleinopathies.

npj Parkinson s DiseaseVol. 10(1)
The University of Sydney (AU), Lund University (SE), Aarhus University (DK), Melanoma Institute Australia (AU)
Michael J. Fox Foundation for Parkinson's Research, Aarhus Universitet, University of Sydney, Lundbeckfonden, Syddansk Universitet, H. Lundbeck A/S
No poverty
Openalex Percentile: Top 13%
Parkinson's Disease Mechanisms and Treatments
1.85
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