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Discriminating α-synuclein strains in Parkinson's disease and multiple system atrophy
Nature. 2020 Feb;578(7794):273-277. doi: 10.1038/s41586-020-1984-7.
Mohammad Shahnawaz 1, Abhisek Mukherjee 1, Sandra Pritzkow # 1, Nicolas Mendez # 1, Prakruti Rabadia 1, Xiangan Liu 2, Bo Hu 2, Ann Schmeichel 3, Wolfgang Singer 3, Gang Wu 4, Ah-Lim Tsai 4, Hamid Shirani 5, K Peter R Nilsson 5, Phillip A Low 3, Claudio Soto 6
Abstract:
...Protein misfolding cyclic amplification (PMCA) is a technique that has previously been used to detect α-synuclein aggregates in samples of cerebrospinal fluid with high sensitivity and specificity7,8. Here we show that the α-synuclein-PMCA assay can discriminate between samples of cerebrospinal fluid from patients diagnosed with Parkinson's disease and samples from patients with multiple system atrophy, with an overall sensitivity of 95.4%. We used a combination of biochemical, biophysical and biological methods to analyse the product of α-synuclein-PMCA, and found that the characteristics of the α-synuclein aggregates in the cerebrospinal fluid could be used to readily distinguish between Parkinson's disease and multiple system atrophy. We also found that the properties of aggregates that were amplified from the cerebrospinal fluid were similar to those of aggregates that were amplified from the brain. These findings suggest that α-synuclein aggregates that are associated with Parkinson's disease and multiple system atrophy correspond to different conformational strains of α-synuclein, which can be amplified and detected by α-synuclein-PMCA. Our results may help to improve our understanding of the mechanism of α-synuclein misfolding and the structures of the aggregates that are implicated in different synucleinopathies, and may also enable the development of a biochemical assay to discriminate between Parkinson's disease and multiple system atrophy.
PMID: 32025029
Free Full-Text: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7066875/