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Apolipoprotein E: a pathological chaperone protein in patients with cerebral and systemic amyloid.

Abstract
Many biochemically diverse proteins can give rise to amyloid fibrils; however, they are all accompanied by P component and glucosaminoglycans. With antibodies specific to apolipoprotein E (apo E) we used immunohistochemical techniques to test for the presence of this protein in both cerebral and systemic amyloid. We found apo E immunoreactivity in all tested types of cerebral and systemic amyloid. In amyloid deposits apo E P, component and glucosaminoglycans may be acting as 'pathological molecular chaperones'. The latter we define as a group of unrelated proteins that induce beta-pleated conformation in amyloidogenic polypeptides.
AuthorsT Wisniewski, B Frangione
JournalNeuroscience letters (Neurosci Lett) Vol. 135 Issue 2 Pg. 235-8 (Feb 03 1992) ISSN: 0304-3940 [Print] Ireland
PMID1625800 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Research Support, U.S. Gov't, P.H.S.)
Chemical References
  • Amyloid
  • Apolipoproteins E
  • Glycosaminoglycans
  • Serum Amyloid P-Component
Topics
  • Amyloid (metabolism)
  • Apolipoproteins E (cerebrospinal fluid, immunology, metabolism)
  • Brain Chemistry (physiology)
  • Glycosaminoglycans (metabolism)
  • Humans
  • Microscopy, Immunoelectron
  • Nervous System Diseases (metabolism, pathology)
  • Paraffin Embedding
  • Serum Amyloid P-Component (metabolism)

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