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The mechanism of Hsp90-induced oligomerization of Tau

Weickert, S.; Wawrzyniuk, M.; John, L.; Rüdiger, S. G. D.; Drescher, M.

2019-11-17 biophysics
10.1101/614289 bioRxiv
Show abstract

Aggregation of the microtubule-associated protein Tau is a hallmark of Alzheimers disease with Tau oligomers suspected as the most toxic agent. Tau is a client of Hsp90, though it is unclear whether and how the chaperone massages the structure of intrinsically disordered Tau. Using electron paramagnetic resonance, we extract structural information from the very broad conformational ensemble of Tau: Tau in solution is highly dynamic and polymorphic, though paper-clip-shaped by long-range contacts. Interaction with Hsp90 promotes an open Tau conformation, which we identify as the molecular basis for the formation of small Tau oligomers by exposure of the aggregation-prone repeat domain to other Tau molecules. At the same time, formation of Tau fibrils is inhibited. We therefore provide the nanometer-scale zoom into chaperoning an amyloid client, highlighting formation of oligomers as the consequence of this biologically relevant interaction.

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