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Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies

Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4351408

Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies

About this item

Full title

Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies

Publisher

London: Nature Publishing Group UK

Journal title

Experimental & molecular medicine, 2015-03, Vol.47 (3), p.e147-e147

Language

English

Formats

Publication information

Publisher

London: Nature Publishing Group UK

More information

Scope and Contents

Contents

Mammalian cells remove misfolded proteins using various proteolytic systems, including the ubiquitin (Ub)-proteasome system (UPS), chaperone mediated autophagy (CMA) and macroautophagy. The majority of misfolded proteins are degraded by the UPS, in which Ub-conjugated substrates are deubiquitinated, unfolded and cleaved into small peptides when pas...

Alternative Titles

Full title

Degradation of misfolded proteins in neurodegenerative diseases: therapeutic targets and strategies

Authors, Artists and Contributors

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4351408

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_4351408

Other Identifiers

ISSN

2092-6413,1226-3613

E-ISSN

2092-6413

DOI

10.1038/emm.2014.117

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