28LQ

Tau filament with S320F mutation

Summary for 28LQ

• Entry DOI: 10.2210/pdb28lq/pdb
• EMDB information: 56601
• Descriptor: Isoform Tau-C of Microtubule-associated protein tau (1 entity in total)
• Functional Keywords: tau, filament, amyloid, s320f, pick's disease, protein fibril
• Biological source: Homo sapiens (human)
• Total number of polymer chains: 4
• Total formula weight: 170908.95

Authors

Qi, C.,Lovestam, S.,Scheres, H.W.S.,Goedert, M. (deposition date: 2026-02-05, release date: 2026-07-29)

Primary citation

Qi, C.,Lovestam, S.,Shi, J.,Murzin, A.G.,Peak-Chew, S.,Warner, T.T.,Seelaar, H.,Cullinane, P.W.,Jaunmuktane, Z.,van Swieten, J.C.,Scheres, S.H.W.,Goedert, M.
The Pick fold in tau filaments from human MAPT mutants.
Acta Neuropathol, 152:-, 2026

PubMed Abstract: Mutations in MAPT, the tau gene, give rise to forms of frontotemporal dementia and parkinsonism linked to chromosome 17 (FTDP-17 T), with abundant filamentous tau inclusions in brain cells. Some mutations that encode missense and deletion variants can give rise to a clinical picture of Pick's disease and filaments made of three-repeat tau in nerve cells. Here we report the electron cryo-microscopy (cryo-EM) structures of tau filaments from the brains of individuals with MAPT mutations D252V, G272V, S320F and ΔG389-I392. The two-layered Pick fold was present in the brains of individuals with mutations D252V and ΔG389-I392 who had also abundant tau inclusions in glial cells. By contrast, mutations G272V and S320F gave rise to a more open variant of the Pick fold, with residues 272-341 rotated by 20-25° with respect to the rest of the structure. These findings show that missense mutations within the filament core can modify the Pick fold, generating closely related structural variants. In addition, we were able to reconstitute the Pick fold and some of its variants using seeded assembly with recombinant 0N3R tau carrying 12 serine or threonine to aspartate substitutions (PAD12) and missense mutations D252V, G272V and S320F. This work provides a foundation for the development of structure-based diagnostic and therapeutic approaches.

PubMed: 42420562
DOI: 10.1007/s00401-026-03049-8

Experimental method

ELECTRON MICROSCOPY (2.8 Å)