npj Parkinson s DiseaseNeurosciencePeer-reviewed journal article
Novel tools to quantify total, phospho-Ser129 and aggregated alpha-synuclein in the mouse brain
Benjamin Guy TristiD, Courtney Jade Wright, Alejandra RangeliD, Louise CottleiD, Asheeta Prasad, Nanna Møller JenseniD, Hjalte GramiD, Nicolas L. DzamkoiD, Poul Henning JenseniD, Deniz KirikiD
Abstract
Assays for quantifying aggregated and phosphorylated (S129) human -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 -synuclein or exhibit poor sensitivity for this target, which is problematic considering the preponderance of mouse models at the forefront of pre-clinical -synuclein research. In this project, we addressed this unmet need by reformulating two existing AlphaLISA(R) SureFire(R) UltraTM total and pS129 -synuclein assay kits to yield robust and ultrasensitive (LLoQ [≤]0.5pg/mL) quantification of mouse and human wild-type and pS129 -synuclein protein. We then employed these assays, together with the BioLegend -synuclein aggregate ELISA, to assess the relationship between -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 -synuclein phosphorylation and aggregation in synucleinopathies.
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