@report{burger_cryo-em_2021,
	title = {Cryo-{EM} structure of alpha-synuclein fibrils amplified by {PMCA} from {PD} and {MSA} patient brains},
	url = {https://biorxiv.org/lookup/doi/10.1101/2021.07.08.451588},
	abstract = {Abstract
          
            Synucleinopathies are neurodegenerative diseases related to the aggregation of the protein alpha-synuclein ({aSyn}). Among these diseases, Parkinson’s disease ({PD}) and multiple system atrophy ({MSA}) are most prevalent. {aSyn} can readily form different fibrillar polymorphs, if exposed to an air-water interface or by templating with pre-existing fibrils. We here report the structures of three fibrillar polymorphs that were obtained after seeding monomeric {aSyn} with {PD} and {MSA} patients brain homogenates using protein misfolding cyclic amplification ({PMCA}). Seeding with a control brain homogenate did not produce fibrils, and seeding with other
            in vitro
            generated fibrillar polymorphs as a control faithfully produced polymorphs of a different type. The here determined fibril structures from {PD} and {MSA} brain tissue represent new folds, which partly resemble that of previously reported
            in vitro
            generated fibrils from Y39 phosphorylated {aSyn} protein. The relevance of these fibrils for synucleinopathies in humans remains to be further investigated.
          
          
            Impact Statement
            Neurodegenerative diseases such as Parkinson’s disease ({PD}) and Multiple System Atrophy ({MSA}) are suspected to be causatively related to the prion-like propagation of aggregates of the protein alpha-synuclein ({aSyn}). The fibril structures reported here were obtained after seeding from diseased human brain homogenate and differ from all previously published {aSyn} fibril arrangements. In case these fibrils would turn out to be the long sought causative agents of these diseases, their structures might lead to the development of therapeutic strategies to modify these diseases and to a better understanding of the mechanistic processes that lead to neurodegeneration and spreading of the diseases.},
	institution = {Neuroscience},
	type = {preprint},
	author = {Burger, Domenic and Fenyi, Alexis and Bousset, Luc and Stahlberg, Henning and Melki, Ronald},
	urldate = {2022-02-17},
	date = {2021-07-09},
	langid = {english},
	doi = {10.1101/2021.07.08.451588},
	keywords = {preprint},
}