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  The proteostasis network and its decline in ageing

Hipp, M. S., Kasturi, P., & Hartl, F. U. (2019). The proteostasis network and its decline in ageing. Nature Reviews Molecular Cell Biology, 20, 421-435. doi:10.1038/s41580-019-0101-y.

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Hipp et al submitted file.pdf (Postprint), 5MB
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https://www.nature.com/articles/s41580-019-0101-y (Verlagsversion)
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 Urheber:
Hipp, Mark S.1, Autor           
Kasturi, Prasad1, Autor           
Hartl, F. Ulrich1, Autor           
Affiliations:
1Hartl, Franz-Ulrich / Cellular Biochemistry, Max Planck Institute of Biochemistry, Max Planck Society, ou_1565152              

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Schlagwörter: Ageing; Chaperones; Protein aggregation; Proteolysis
 Zusammenfassung: Ageing is a major risk factor for the development of many diseases, prominently including neurodegenerative disorders such as Alzheimer disease and Parkinson disease. A hallmark of many age-related diseases is the dysfunction in protein homeostasis (proteostasis), leading to the accumulation of protein aggregates. In healthy cells, a complex proteostasis network, comprising molecular chaperones and proteolytic machineries and their regulators, operates to ensure the maintenance of proteostasis. These factors coordinate protein synthesis with polypeptide folding, the conservation of protein conformation and protein degradation. However, sustaining proteome balance is a challenging task in the face of various external and endogenous stresses that accumulate during ageing. These stresses lead to the decline of proteostasis network capacity and proteome integrity. The resulting accumulation of misfolded and aggregated proteins affects, in particular, postmitotic cell types such as neurons, manifesting in disease. Recent analyses of proteome-wide changes that occur during ageing inform strategies to improve proteostasis. The possibilities of pharmacological augmentation of the capacity of proteostasis networks hold great promise for delaying the onset of age-related pathologies associated with proteome deterioration and for extending healthspan.

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 Datum: 2019-022019-07
 Publikationsstatus: Erschienen
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 Identifikatoren: DOI: 10.1038/s41580-019-0101-y
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Projektname : GA ERC-2012-SyG_318987–ToPAG
Grant ID : 318987
Förderprogramm : Funding Programme 7 (FP7)
Förderorganisation : European Commission (EC)

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Titel: Nature Reviews Molecular Cell Biology
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: London, UK : Nature Pub. Group
Seiten: - Band / Heft: 20 Artikelnummer: - Start- / Endseite: 421 - 435 Identifikator: ISSN: 1471-0072
CoNE: https://pure.mpg.de/cone/journals/resource/110985821000941