Jackson, MP and Hewitt, EW orcid.org/0000-0002-6238-6303 (2016) Cellular proteostasis: degradation of misfolded proteins by lysosomes. Essays in Biochemistry, 60 (2). pp. 173-180. ISSN 0071-1365
Abstract
Proteostasis refers to the regulation of the cellular concentration, folding, interactions and localisation of each of the proteins that comprise the proteome. One essential element of proteostasis is the disposal of misfolded proteins by the cellular pathways of protein degradation. Lysosomes are an important site for the degradation of misfolded proteins, which are trafficked to this organelle by the pathways of macroautophagy, chaperone mediated autophagy and endocytosis. Conversely, amyloid diseases represent a failure in proteostasis, in which proteins misfold forming amyloid deposits that are not degraded effectively by cells. Amyloid may then exacerbate this failure by disrupting autophagy and lysosomal proteolysis. However, targeting the pathways that regulate autophagy and the biogenesis of lysosomes may present approaches that can rescue cells from the deleterious effects of amyloidogenic proteins.
Metadata
Item Type: | Article |
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Authors/Creators: |
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Copyright, Publisher and Additional Information: | © 2016 The Author(s). This is an open access article published by Portland Press Limited on behalf of the Biochemical Society and distributed under the Creative Commons Attribution Licence 4.0 (CC BY). |
Keywords: | amyloid; α-synuclein; autophagy; β2-microglobulin; chaperone mediated autophagy; immunoglobulin light chain; lysosome; macroautophagy; mTOR; Parkinson’s; protein aggregation; protein misfolding; proteostasis; rapamycin; TFEB |
Dates: |
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Institution: | The University of Leeds |
Academic Units: | The University of Leeds > Faculty of Biological Sciences (Leeds) > School of Molecular and Cellular Biology (Leeds) |
Funding Information: | Funder Grant number Wellcome Trust 092896/Z/10/Z |
Depositing User: | Symplectic Publications |
Date Deposited: | 10 May 2016 10:51 |
Last Modified: | 23 Jun 2023 22:05 |
Published Version: | https://doi.org/10.1042/EBC20160005 |
Status: | Published |
Publisher: | Portland Press |
Identification Number: | 10.1042/EBC20160005 |
Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:99503 |