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TitleStructures of α-synuclein filaments from multiple system atrophy.
Journal, issue, pagesNature, Vol. 585, Issue 7825, Page 464-469, Year 2020
Publish dateMay 27, 2020
AuthorsManuel Schweighauser / Yang Shi / Airi Tarutani / Fuyuki Kametani / Alexey G Murzin / Bernardino Ghetti / Tomoyasu Matsubara / Taisuke Tomita / Takashi Ando / Kazuko Hasegawa / Shigeo Murayama / Mari Yoshida / Masato Hasegawa / Sjors H W Scheres / Michel Goedert /
PubMed AbstractSynucleinopathies, which include multiple system atrophy (MSA), Parkinson's disease, Parkinson's disease with dementia and dementia with Lewy bodies (DLB), are human neurodegenerative diseases. ...Synucleinopathies, which include multiple system atrophy (MSA), Parkinson's disease, Parkinson's disease with dementia and dementia with Lewy bodies (DLB), are human neurodegenerative diseases. Existing treatments are at best symptomatic. These diseases are characterized by the presence of, and believed to be caused by the formation of, filamentous inclusions of α-synuclein in brain cells. However, the structures of α-synuclein filaments from the human brain are unknown. Here, using cryo-electron microscopy, we show that α-synuclein inclusions from the brains of individuals with MSA are made of two types of filament, each of which consists of two different protofilaments. In each type of filament, non-proteinaceous molecules are present at the interface of the two protofilaments. Using two-dimensional class averaging, we show that α-synuclein filaments from the brains of individuals with MSA differ from those of individuals with DLB, which suggests that distinct conformers or strains characterize specific synucleinopathies. As is the case with tau assemblies, the structures of α-synuclein filaments extracted from the brains of individuals with MSA differ from those formed in vitro using recombinant proteins, which has implications for understanding the mechanisms of aggregate propagation and neurodegeneration in the human brain. These findings have diagnostic and potential therapeutic relevance, especially because of the unmet clinical need to be able to image filamentous α-synuclein inclusions in the human brain.
External linksNature / PubMed:32461689 / PubMed Central
MethodsEM (helical sym.)
Resolution2.6 - 3.29 Å
Structure data

10650

6xyo

EMDB-10650, PDB-6xyo:
Multiple system atrophy Type I alpha-synuclein filament
Method: EM (helical sym.) / Resolution: 2.6 Å

10651

6xyp

EMDB-10651, PDB-6xyp:
Multiple system atrophy Type II-1 alpha-synuclein filament
Method: EM (helical sym.) / Resolution: 3.29 Å

10652

6xyq

EMDB-10652, PDB-6xyq:
Multiple system atrophy Type II-2 alpha-synuclein filament
Method: EM (helical sym.) / Resolution: 3.09 Å

Source
  • homo sapiens (human)
KeywordsPROTEIN FIBRIL / multiple system atrophy / alpha-synuclein filament

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