Structure and pro-toxic mechanism of the human Hsp90/PPIase/Tau complex
2018 | journal article. A publication with affiliation to the University of Göttingen.
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Structure and pro-toxic mechanism of the human Hsp90/PPIase/Tau complex
Oroz, J.; Chang, B. J.; Wysoczanski, P.; Lee, C.-T.; Pérez-Lara, Á.; Chakraborty, P. & Hofele, R. V. et al. (2018)
Nature Communications, 9(1) art. 4532. DOI: https://doi.org/10.1038/s41467-018-06880-0
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Details
- Authors
- Oroz, Javier; Chang, Bliss J.; Wysoczanski, Piotr; Lee, Chung-Tien; Pérez-Lara, Ángel; Chakraborty, Pijush; Hofele, Romina V.; Baker, Jeremy D.; Blair, Laura J.; Biernat, Jacek; Urlaub, Henning; Mandelkow, Eckhard; Dickey, Chad A.; Zweckstetter, Markus
- Abstract
- The molecular chaperone Hsp90 is critical for the maintenance of cellular homeostasis and represents a promising drug target. Despite increasing knowledge on the structure of Hsp90, the molecular basis of substrate recognition and pro-folding by Hsp90/co-chaperone complexes remains unknown. Here, we report the solution structures of human full-length Hsp90 in complex with the PPIase FKBP51, as well as the 280 kDa Hsp90/FKBP51 complex bound to the Alzheimer's disease-related protein Tau. We reveal that the FKBP51/Hsp90 complex, which synergizes to promote toxic Tau oligomers in vivo, is highly dynamic and stabilizes the extended conformation of the Hsp90 dimer resulting in decreased Hsp90 ATPase activity. Within the ternary Hsp90/FKBP51/Tau complex, Hsp90 serves as a scaffold that traps the PPIase and nucleates multiple conformations of Tau's proline-rich region next to the PPIase catalytic pocket in a phosphorylation-dependent manner. Our study defines a conceptual model for dynamic Hsp90/co-chaperone/client recognition.
- Issue Date
- 2018
- Journal
- Nature Communications
- Project
- info:eu-repo/grantAgreement/EC/FP7/626526/EU//HSP70-TAU NMR
info:eu-repo/grantAgreement/EC/FP7/283570/EU//BIOSTRUCT-X - Organization
- Deutsches Zentrum für Neurodegenerative Erkrankungen (DZNE) ; Max-Planck-Institut für Biophysikalische Chemie ; Institut für Klinische Chemie
- ISSN
- 2041-1723
- Language
- English