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ER-associated degradation: Protein quality control and beyond

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JOURNAL OF CELL BIOLOGY
卷 204, 期 6, 页码 868-878

出版社

ROCKEFELLER UNIV PRESS
DOI: 10.1083/jcb.201312042

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资金

  1. CRG internal funds
  2. grant of the Spanish MCCIN
  3. ERC starting grant
  4. International Early Career Award from the Howard Hughes Medical Institute
  5. La Caixa graduate fellowship

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Even with the assistance of many cellular factors, a significant fraction of newly synthesized proteins ends up mis-folded. Cells evolved protein quality control systems to ensure that these potentially toxic species are detected and eliminated. The best characterized of these pathways, the ER-associated protein degradation (ERAD), monitors the folding of membrane and secretory proteins whose biogenesis takes place in the endoplasmic reticulum (ER). There is also increasing evidence that ERAD controls other ER-related functions through regulated degradation of certain folded ER proteins, further highlighting the role of ERAD in cellular homeostasis.

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