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Mechanisms and Functions of Spatial Protein Quality Control.
Sontag, Emily Mitchell; Samant, Rahul S; Frydman, Judith.
Affiliation
  • Sontag EM; Department of Biology, Stanford University, Stanford, California 94305; email: emsontag@stanford.edu , rsamant@stanford.edu , jfrydman@stanford.edu.
  • Samant RS; Department of Biology, Stanford University, Stanford, California 94305; email: emsontag@stanford.edu , rsamant@stanford.edu , jfrydman@stanford.edu.
  • Frydman J; Department of Biology, Stanford University, Stanford, California 94305; email: emsontag@stanford.edu , rsamant@stanford.edu , jfrydman@stanford.edu.
Annu Rev Biochem ; 86: 97-122, 2017 06 20.
Article in En | MEDLINE | ID: mdl-28489421
A healthy proteome is essential for cell survival. Protein misfolding is linked to a rapidly expanding list of human diseases, ranging from neurodegenerative diseases to aging and cancer. Many of these diseases are characterized by the accumulation of misfolded proteins in intra- and extracellular inclusions, such as amyloid plaques. The clear link between protein misfolding and disease highlights the need to better understand the elaborate machinery that manages proteome homeostasis, or proteostasis, in the cell. Proteostasis depends on a network of molecular chaperones and clearance pathways involved in the recognition, refolding, and/or clearance of aberrant proteins. Recent studies reveal that an integral part of the cellular management of misfolded proteins is their spatial sequestration into several defined compartments. Here, we review the properties, function, and formation of these compartments. Spatial sequestration plays a central role in protein quality control and cellular fitness and represents a critical link to the pathogenesis of protein aggregation-linked diseases.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aging / Molecular Chaperones / Neurodegenerative Diseases / Proteostasis Deficiencies / Protein Aggregation, Pathological Limits: Humans Language: En Journal: Annu Rev Biochem Year: 2017 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Aging / Molecular Chaperones / Neurodegenerative Diseases / Proteostasis Deficiencies / Protein Aggregation, Pathological Limits: Humans Language: En Journal: Annu Rev Biochem Year: 2017 Type: Article