articleAnnual Review of BiochemistryApr 25, 2017Closed access

Protein Misfolding Diseases

Max Planck Institute of Biochemistry

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Abstract

The majority of protein molecules must fold into defined three-dimensional structures to acquire functional activity. However, protein chains can adopt a multitude of conformational states, and their biologically active conformation is often only marginally stable. Metastable proteins tend to populate misfolded species that are prone to forming toxic aggregates, including soluble oligomers and fibrillar amyloid deposits, which are linked with neurodegeneration in Alzheimer and Parkinson disease, and many other pathologies. To prevent or regulate protein aggregation, all cells contain an extensive protein homeostasis (or proteostasis) network comprising molecular chaperones and other factors. These defense…

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551
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Authors

1

Topics & keywords

Keywords
  • Proteostasis
  • Protein folding
  • Neurodegeneration
  • Protein aggregation
  • Amyloid (mycology)
  • Protein structure
  • Chemistry
  • Biology
UN Sustainable Development Goals
  • Life in Land
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