Author:
Trist Benjamin Guy,Wright Courtney Jade,Rangel Alejandra,Cottle Louise,Prasad Asheeta,Jensen Nanna Møller,Gram Hjalte,Dzamko Nicolas,Jensen Poul Henning,Kirik Deniz
Abstract
AbstractAssays 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®SureFire®UltraTMtotal and pS129 α-synuclein assay kits to yield robust and ultrasensitive (LLoQ ≤0.5pg/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 the relationship between 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.
Publisher
Cold Spring Harbor Laboratory