Nature Communications (Mar 2021)

Cryo-EM structure of amyloid fibrils formed by the entire low complexity domain of TDP-43

  • Qiuye Li,
  • W. Michael Babinchak,
  • Witold K. Surewicz

DOI
https://doi.org/10.1038/s41467-021-21912-y
Journal volume & issue
Vol. 12, no. 1
pp. 1 – 8

Abstract

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Amyotrophic lateral sclerosis (ALS) and frontotemporal lobar degeneration (FTLD) patients have brain deposits with amyloid-like aggregates from large C-terminal fragments of the transactive response DNA-binding protein of 43 kDa (TDP-43). Here, the authors present the cryo-EM structure of amyloid fibrils generated from the complete C-terminal TDP-43 low complexity domain and they discuss the effects of disease-causing mutations and phosphorylation of specific Ser residues.