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. Author manuscript; available in PMC: 2020 Mar 12.
Published in final edited form as: Nature. 2020 Feb 5;578(7794):273–277. doi: 10.1038/s41586-020-1984-7

Extended Data Fig. 6 |. Proteinase K digestion profiles of α-syn aggregates after several rounds of α-syn-PMCA.

Extended Data Fig. 6 |

This is the same experiment as Fig. 2e, showing the results obtained with samples from different patients with PD (n = 3) and patients with MSA (n = 3). The first round corresponds to direct amplification from the CSF of the patients. For the second round of amplification, aggregates produced in the first round were diluted 100-fold into fresh α-syn monomer substrate and a new round of α-syn-PMCA was performed. The assay was then repeated for the third and fourth rounds using amplified α-syn aggregates (1%) from the previous round. Amplified aggregates were treated with proteinase K (1 mg ml−1) for 1 h and proteins were separated on a 12% Bis-Tris gel and immunoblotted with the BD anti-α-syn clone 42 antibody. Molecular weight markers (kDa) are indicated on the left of the blot.