Hsp70 - a master regulator in protein degradation.
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.
Mots clés
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