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Protein disaggregation machineries in the human cytosol.
Wentink, Anne; Rosenzweig, Rina.
Afiliação
  • Wentink A; Leiden Institute of Chemistry, Leiden University, Einsteinweg 55, 2333 CC Leiden, Netherlands. Electronic address: rina.rosenzweig@weizmann.ac.il.
  • Rosenzweig R; Chemical and Structural Biology Department, Weizmann Institute of Science, Rehovot, 761000, Israel. Electronic address: a.s.wentink@lic.leidenuniv.nl.
Curr Opin Struct Biol ; 83: 102735, 2023 Dec.
Article em En | MEDLINE | ID: mdl-38000128
ABSTRACT
Proteins carry out the vast majority of functions in cells, but can only do so when properly folded. Following stress or mutation, proteins can lose their proper fold, resulting in misfolding, inactivity, and aggregation-posing a threat to cellular health. In order to counteract protein aggregation, cells have evolved a remarkable subset of molecular chaperones, called protein disaggregases, which collaboratively possess the ability to forcibly untangle protein aggregates. Here, we review the different chaperone disaggregation machineries present in the human cytosol and their mechanisms of action. Understanding, how these disaggregases function, is both universally and clinically important, as protein aggregation has been linked to multiple, debilitating neurodegenerative diseases.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Choque Térmico HSP70 / Agregados Proteicos Limite: Humans Idioma: En Revista: Curr Opin Struct Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Proteínas de Choque Térmico HSP70 / Agregados Proteicos Limite: Humans Idioma: En Revista: Curr Opin Struct Biol Assunto da revista: BIOLOGIA MOLECULAR Ano de publicação: 2023 Tipo de documento: Article