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• W2023342524 abstract "Prion diseases comprise a family of fatal neurodegenerative disorders caused by the conformational re-arrangement of a normal host-encoded protein, PrPC, to an abnormal infectious isoform termed PrPSc. Currently, the precise cellular mechanism(s) underlying prion disease pathogenesis remain unclear. Evidence suggests a role for the ubiquitin proteasome system (UPS), a protein degradation pathway that is critical for maintaining cellular proteostasis. Dysfunction of the UPS has been implicated in various neurodegenerative diseases. However, the mechanisms of this impairment remain unknown in many cases, and evidence that disease-associated misfolded proteins are able to directly inhibit the function of the proteasome has been lacking. Recently, we have shown data describing a mechanism of proteasome impairment by the direct interaction of β-sheet-rich PrP to reduce gate opening and inhibit substrate entry. This novel mechanism may provide a model for how other misfolded, disease-associated proteins might interact with the proteasome to disrupt its function. Targeting the UPS to restore proteostasis in neurodegenerative disorders in which misfolded proteins accumulate offers a possible target for therapeutic intervention." @default.
• W2023342524 created "2016-06-24" @default.
• W2023342524 creator A5027651702 @default.
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• W2023342524 date "2012-01-01" @default.
• W2023342524 modified "2023-09-26" @default.
• W2023342524 title "Misfolded PrP and a novel mechanism of proteasome inhibition" @default.
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• W2023342524 doi "https://doi.org/10.4161/pri.6.1.18272" @default.
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