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PMID: 14685250 Published · ppublish English Journal Article Review

Protein degradation and protection against misfolded or damaged proteins.

Nature ·Vol. 426 ·No. 6968 ·2003-12-18 ·Pages 895-9

Goldberg AL

Abstract

The ultimate mechanism that cells use to ensure the quality of intracellular proteins is the selective destruction of misfolded or damaged polypeptides. In eukaryotic cells, the large ATP-dependent proteolytic machine, the 26S proteasome, prevents the accumulation of non-functional, potentially toxic proteins. This process is of particular importance in protecting cells against harsh conditions (for example, heat shock or oxidative stress) and in a variety of diseases (for example, cystic fibrosis and the major neurodegenerative diseases). A full understanding of the pathogenesis of the protein-folding diseases will require greater knowledge of how misfolded proteins are recognized and selectively degraded.

MeSH Terms
Humans Peptide Hydrolases/metabolism Proteasome Endopeptidase Complex Protein Biosynthesis Protein Denaturation Protein Folding Protein Processing, Post-Translational Proteins/chemistry,metabolism Ubiquitin/metabolism
Chemicals
Proteins Ubiquitin Peptide Hydrolases Proteasome Endopeptidase Complex ATP dependent 26S protease
Authors & Affiliations
1 authors, click to expand affiliations / ORCID
Goldberg Alfred L
Department of Cell Biology, Harvard Medical School, Boston, Massachusetts 02115, USA. alfred_goldberg@hms.harvard.edu
Article Info
Journal
Nature
Abbr.
Nature
ISSN
1476-4687
Published
2003-12-18
Pages
895-9
Language
English
Region
England
NLM ID
0410462
Subset
IM
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