Design and development of non-fibrillar amyloid beta as a potential Alzheimer vaccine

Biochem Biophys Res Commun. 2010 Apr 2;394(2):393-7. doi: 10.1016/j.bbrc.2010.03.031. Epub 2010 Mar 7.

Abstract

Alzheimer's disease (AD) is the most common cause of dementia affecting the elderly. Treatment for effective cure of this complex neurodegenerative disease does not yet exist. In AD, otherwise soluble, monomeric form of amyloid beta (Abeta) peptide converts into toxic, fibrillar form rich in beta-sheet content. Several immunological approaches that prevent this conversion of Abeta into pathological form or that accelerate its clearance are being actively pursued worldwide. As part of these attempts, we report here, the design and characterization of a non-amyloidogenic homologue of Abeta (Abeta-KEK). We demonstrate that this peptide is helical in nature and retains the immunoneutralizing epitopes of native Abeta. More importantly, Fab fragments of the polyclonal anti-Abeta-KEK antibodies interfere with formation of Abeta fibrils as well as dissociate the preformed Abeta aggregates in vitro. These results suggest that non-amyloidogenic Abeta-KEK may serve as a safer alternative vaccine for Alzheimer's disease.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alzheimer Disease / prevention & control*
  • Alzheimer Vaccines / chemistry
  • Alzheimer Vaccines / immunology*
  • Amino Acid Sequence
  • Amyloid beta-Peptides / chemistry
  • Amyloid beta-Peptides / immunology*
  • Antibodies / immunology
  • Humans
  • Immunodominant Epitopes / chemistry
  • Immunodominant Epitopes / immunology*
  • Immunoglobulin Fab Fragments / immunology
  • Molecular Sequence Data
  • Peptides / chemistry
  • Peptides / immunology
  • Protein Structure, Secondary

Substances

  • Alzheimer Vaccines
  • Amyloid beta-Peptides
  • Antibodies
  • Immunodominant Epitopes
  • Immunoglobulin Fab Fragments
  • Peptides