CryoET of β-amyloid and tau within postmortem Alzheimer's disease brain

Nature. 2024 Jul;631(8022):913-919. doi: 10.1038/s41586-024-07680-x. Epub 2024 Jul 10.

Abstract

A defining pathological feature of most neurodegenerative diseases is the assembly of proteins into amyloid that form disease-specific structures1. 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.

MeSH terms

  • Alzheimer Disease* / metabolism
  • Alzheimer Disease* / pathology
  • Amyloid beta-Peptides* / chemistry
  • Amyloid beta-Peptides* / metabolism
  • Amyloid beta-Peptides* / ultrastructure
  • Autopsy
  • Brain* / metabolism
  • Brain* / pathology
  • Brain* / ultrastructure
  • Cryoelectron Microscopy*
  • Electron Microscope Tomography*
  • Extracellular Vesicles / chemistry
  • Extracellular Vesicles / metabolism
  • Extracellular Vesicles / ultrastructure
  • Humans
  • Male
  • Mice
  • Plaque, Amyloid* / chemistry
  • Plaque, Amyloid* / metabolism
  • Plaque, Amyloid* / pathology
  • Plaque, Amyloid* / ultrastructure
  • tau Proteins* / chemistry
  • tau Proteins* / metabolism
  • tau Proteins* / ultrastructure

Substances

  • Amyloid beta-Peptides
  • tau Proteins
  • MAPT protein, human
  • APP protein, human