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Hsp70 - a master regulator in protein degradation.
Fernández-Fernández, María Rosario; Gragera, Marcos; Ochoa-Ibarrola, Lissette; Quintana-Gallardo, Lucía; Valpuesta, José María.
Affiliation
  • Fernández-Fernández MR; Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
  • Gragera M; Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
  • Ochoa-Ibarrola L; Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
  • Quintana-Gallardo L; Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
  • Valpuesta JM; Centro Nacional de Biotecnología (CNB-CSIC), Madrid, Spain.
FEBS Lett ; 591(17): 2648-2660, 2017 09.
Article de En | MEDLINE | ID: mdl-28696498
Proteostasis, the controlled balance of protein synthesis, folding, assembly, trafficking and degradation, is a paramount necessity for cell homeostasis. Impaired proteostasis is a hallmark of ageing and of many human diseases. Molecular chaperones are essential for proteostasis in eukaryotic cells, and their function has traditionally been linked to protein folding, assembly and disaggregation. More recent findings suggest that chaperones also contribute to key steps in protein degradation. In particular, Hsp70 has an essential role in substrate degradation through the ubiquitin-proteasome system, as well as through different autophagy pathways. Accumulated knowledge suggests that the fate of an Hsp70 substrate is dictated by the combination of partners (cochaperones and other chaperones) that interact with Hsp70 in a given cell context.
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Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines du choc thermique HSP70 / Protéolyse Limites: Animals / Humans Langue: En Journal: FEBS Lett Année: 2017 Type de document: Article Pays d'affiliation: Espagne Pays de publication: Royaume-Uni

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Protéines du choc thermique HSP70 / Protéolyse Limites: Animals / Humans Langue: En Journal: FEBS Lett Année: 2017 Type de document: Article Pays d'affiliation: Espagne Pays de publication: Royaume-Uni