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000148122 1001_ $$aAkoury, E.
000148122 1101_ $$aDESY$$bExperiments with synchrotron radiation
000148122 245__ $$aInhibition of tau filament formation by conformational modulation
000148122 260__ $$aWashington, DC$$bAmerican Chemical Society$$c2013
000148122 300__ $$a2853-2862
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000148122 440_0 $$0PERI:(DE-600)1472210-0$$aJ. Am. Chem. Soc.$$v135$$x0002-7863$$y7
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000148122 520__ $$aAntiaggregation drugs play an important role in therapeutic approaches for Alzheimer's disease. Although a large number of small molecules that inhibit the aggregation of the tau protein have been identified, little is known about their mode of action. Here, we reveal the mechanism and the nature of tau species that are generated by interaction of tau with the organic compound pthalocyanine tetrasulfonate (PcTS). We demonstrate that PcTS interferes with tau filament formation by targeting the protein into soluble oligomers. A combination of NMR spectroscopy, electron paramagnetic resonance, and small-angle X-ray scattering reveals that the soluble tau oligomers contain a dynamic, noncooperatively stabilized core with a diameter of 30-40 nm that is distinct from the core of tau filaments. Our results suggest that specific modulation of the conformation of tau is a viable strategy for reduction of pathogenic tau deposits.
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000148122 7001_ $$aGajda, M. J.
000148122 7001_ $$aPickhardt, M.
000148122 7001_ $$aBiernat, J.
000148122 7001_ $$aPornsuwan, S.
000148122 7001_ $$aGriesinger, Ch.
000148122 7001_ $$aMandelkow, E.
000148122 7001_ $$aZweckstetter, M.
000148122 773__ $$0PERI:(DE-600)1472210-0$$a10.1021/ja312471h$$gVol. 135, p. 2853-2862$$p2853-2862$$q135<2853-2862$$tJournal of the American Chemical Society$$v135$$x0002-7863$$y2013
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000148122 9141_ $$a(c) American Chemical Society. Post Referee-Version 12 Monate gesperrt (bis Feb. 2014). Code P.$$y2013
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