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dc.contributor.authorSebastian, Rebecca M
dc.contributor.authorShoulders, Matthew D
dc.date.accessioned2021-10-27T20:34:45Z
dc.date.available2021-10-27T20:34:45Z
dc.date.issued2020
dc.identifier.urihttps://hdl.handle.net/1721.1/136294
dc.description.abstract© 2020 Annual Reviews Inc.. All rights reserved. Protein folding in the cell is mediated by an extensive network of >1,000 chaperones, quality control factors, and trafficking mechanisms collectively termed the proteostasis network. While the components and organization of this network are generally well established, our understanding of how protein-folding problems are identified, how the network components integrate to successfully address challenges, and what types of biophysical issues each proteostasis network component is capable of addressing remains immature. We describe a chemical biology-informed framework for studying cellular proteostasis that relies on selection of interesting protein-folding problems and precise researcher control of proteostasis network composition and activities. By combining these methods with multifaceted strategies to monitor protein folding, degradation, trafficking, and aggregation in cells, researchers continue to rapidly generate new insights into cellular proteostasis.
dc.language.isoen
dc.publisherAnnual Reviews
dc.relation.isversionof10.1146/ANNUREV-BIOCHEM-013118-111552
dc.rightsCreative Commons Attribution-Noncommercial-Share Alike
dc.rights.urihttp://creativecommons.org/licenses/by-nc-sa/4.0/
dc.sourcePMC
dc.titleChemical Biology Framework to Illuminate Proteostasis
dc.typeArticle
dc.relation.journalAnnual Review of Biochemistry
dc.eprint.versionAuthor's final manuscript
dc.type.urihttp://purl.org/eprint/type/JournalArticle
eprint.statushttp://purl.org/eprint/status/PeerReviewed
dc.date.updated2021-07-07T16:25:47Z
dspace.orderedauthorsSebastian, RM; Shoulders, MD
dspace.date.submission2021-07-07T16:25:48Z
mit.journal.volume89
mit.journal.issue1
mit.licenseOPEN_ACCESS_POLICY
mit.metadata.statusAuthority Work and Publication Information Needed


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