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TitleCryoET of β-amyloid and tau within postmortem Alzheimer's disease brain.
Journal, issue, pagesNature, Year 2024
Publish dateJul 10, 2024
AuthorsMadeleine A G Gilbert / Nayab Fatima / Joshua Jenkins / Thomas J O'Sullivan / Andreas Schertel / Yehuda Halfon / Martin Wilkinson / Tjado H J Morrema / Mirjam Geibel / Randy J Read / Neil A Ranson / Sheena E Radford / Jeroen J M Hoozemans / René A W Frank /
PubMed AbstractA defining pathological feature of most neurodegenerative diseases is the assembly of proteins into amyloid that form disease-specific structures. In Alzheimer's disease, this is characterized by the ...A defining pathological feature of most neurodegenerative diseases is the assembly of proteins into amyloid that form disease-specific structures. In Alzheimer's disease, this is characterized by the deposition of β-amyloid and tau with disease-specific conformations. The in situ structure of amyloid in the human brain is unknown. Here, using cryo-fluorescence microscopy-targeted cryo-sectioning, cryo-focused ion beam-scanning electron microscopy lift-out and cryo-electron tomography, we determined in-tissue architectures of β-amyloid and tau pathology in a postmortem Alzheimer's disease donor brain. β-amyloid plaques contained a mixture of fibrils, some of which were branched, and protofilaments, arranged in parallel arrays and lattice-like structures. Extracellular vesicles and cuboidal particles defined the non-amyloid constituents of β-amyloid plaques. By contrast, tau inclusions formed parallel clusters of unbranched filaments. Subtomogram averaging a cluster of 136 tau filaments in a single tomogram revealed the polypeptide backbone conformation and filament polarity orientation of paired helical filaments within tissue. Filaments within most clusters were similar to each other, but were different between clusters, showing amyloid heterogeneity that is spatially organized by subcellular location. The in situ structural approaches outlined here for human donor tissues have applications to a broad range of neurodegenerative diseases.
External linksNature / PubMed:38987603
MethodsEM (helical sym.) / EM (subtomogram averaging)
Resolution3.0 - 33.0 Å
Structure data

EMDB-18990: CryoEM map of tau PHF sarkosyl-extracted from a human AD patient (associated with in situ tomography)
Method: EM (helical sym.) / Resolution: 3.0 Å

EMDB-50148: Tau PHF subtomogram average relating to CS1 extended data Figure 9A
Method: EM (subtomogram averaging) / Resolution: 32.64 Å

EMDB-50152: Tau PHF subtomogram average relating to CS2 Figure 3i-j.
Method: EM (subtomogram averaging) / Resolution: 8.7 Å

EMDB-50153: Tau PHF subtomogram average relating to CS3 extended data Figure 9c
Method: EM (subtomogram averaging) / Resolution: 19.04 Å

EMDB-50155: Tau PHF subtomogram average relating to CS4 extended data Figure 9d
Method: EM (subtomogram averaging) / Resolution: 28.56 Å

EMDB-50156: Tau PHF subtomogram average relating to CS5 extended data Figure 9b
Method: EM (subtomogram averaging) / Resolution: 20.77 Å

EMDB-50157: Tau PHF subtomogram average relating to CS6 extended data Figure 9e
Method: EM (subtomogram averaging) / Resolution: 33.0 Å

EMDB-50159: Tau PHF subtomogram average relating to CS7 extended data Figure 9f
Method: EM (subtomogram averaging) / Resolution: 25.0 Å

EMDB-50160: Tau PHF subtomogram average relating to LOL1_PHF Figure 4g-h
Method: EM (subtomogram averaging) / Resolution: 19.4 Å

EMDB-50161: Tau SF subtomogram average relating to LOL1_SF Figure 4g-h
Method: EM (subtomogram averaging) / Resolution: 19.0 Å

EMDB-50162: Tau SF subtomogram average relating to LOL2_SF Figure 4i-j
Method: EM (subtomogram averaging) / Resolution: 19.0 Å

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  • Homo sapiens (human)

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