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  Kinetically distinct phases of tau on microtubules regulate kinesin motors and severing enzymes.

Siahaan, V., Krattenmacher, J., Hyman, A., Diez, S., Hernández-Vega, A., Lansky, Z., et al. (2019). Kinetically distinct phases of tau on microtubules regulate kinesin motors and severing enzymes. Nature cell biology, 21(9), 1086-1092. doi:10.1038/s41556-019-0374-6.

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Siahaan, Valerie, Autor
Krattenmacher, Jochen, Autor
Hyman, Anthony1, Autor           
Diez, Stefan1, Autor           
Hernández-Vega, Amayra1, Autor           
Lansky, Zdenek1, Autor           
Braun, Marcus1, Autor           
Affiliations:
1Max Planck Institute for Molecular Cell Biology and Genetics, Max Planck Society, ou_2340692              

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 Zusammenfassung: Tau is an intrinsically disordered protein, which diffuses on microtubules1. In neurodegenerative diseases, collectively termed tauopathies, malfunction of tau and its detachment from axonal microtubules are correlated with axonal degeneration2. Tau can protect microtubules from microtubule-degrading enzymes such as katanin3. However, how tau carries out this regulatory function is still unclear. Here, using in vitro reconstitution, we show that tau molecules on microtubules cooperatively form cohesive islands that are kinetically distinct from tau molecules that individually diffuse on microtubules. Dependent on the tau concentration in solution, the islands reversibly grow or shrink by addition or release of tau molecules at their boundaries. Shielding microtubules from kinesin-1 motors and katanin, the islands exhibit regulatory qualities distinct from a comparably dense layer of diffusible tau. Superprocessive kinesin-8 motors penetrate the islands and cause their disassembly. Our results reveal a microtubule-dependent phase of tau that constitutes an adaptable protective layer on the microtubule surface. We anticipate that other intrinsically disordered axonal proteins display a similar cooperative behaviour and potentially compete with tau in regulating access to the microtubule surface.

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 Datum: 2019-09-01
 Publikationsstatus: Erschienen
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 Identifikatoren: DOI: 10.1038/s41556-019-0374-6
Anderer: cbg-7510
PMID: 31481789
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Titel: Nature cell biology
  Andere : Nat Cell Biol
Genre der Quelle: Zeitschrift
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Seiten: - Band / Heft: 21 (9) Artikelnummer: - Start- / Endseite: 1086 - 1092 Identifikator: -