Protein aggregation as a cause for disease

T. Scheibel, J. Buchner

Research output: Chapter in Book/Report/Conference proceedingChapterpeer-review

6 Scopus citations

Abstract

The ability of proteins to fold into a defined and functional conformation is one of the most fundamental processes in biology. Certain conditions, however, initiate misfolding or unfolding of proteins. This leads to the loss of functional protein or it can result in a wide range of diseases. One group of diseases, which includes Alzheimer's, Parkinson's, Huntington's disease, and the transmissible spongiform encephalopathies (prion diseases), involves deposition of aggregated proteins. Normally, such protein aggregates are not found in properly functioning biological systems, because a variety of mechanisms inhibit their formation. Understanding the nature of these protective mechanisms together with the understanding of factors reducing or deactivating the natural protection machinery will be crucial for developing strategies to prevent and treat these disastrous diseases.

Original languageEnglish
Title of host publicationMolecular Chaperones in Health and Disease
PublisherSpringer Science and Business Media, LLC
Pages199-219
Number of pages21
ISBN (Print)9783540258759
DOIs
StatePublished - 2006

Publication series

NameHandbook of Experimental Pharmacology
Volume172
ISSN (Print)0171-2004
ISSN (Electronic)1865-0325

Keywords

  • Alzheimer
  • Amyloid
  • Huntington
  • Parkinson
  • Prion
  • Protein deposits
  • Quality control
  • Toxic species

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