Leveraging an extensive panel of α-synuclein antibodies that targets a wide range of epitopes, the authors provide evidence that multiple system atrophy α-synuclein inclusions display distinct misfolded strain-like characteristics divergent from Lewy body diseases. The findings also indicate that in multiple system atrophy α-synuclein prion-like strains are likely inherently mutable.
- Jess-Karan S. Dhillon
- Jorge A. Trejo-Lopez
- Anthony T. Yachnis
