Amino-terminal deletions enhance aggregation of beta-amyloid peptides in vitro

J Biol Chem. 1995 Oct 13;270(41):23895-8. doi: 10.1074/jbc.270.41.23895.

Abstract

beta-Amyloid protein, which assembles into pathological aggregates deposited in Alzheimer's disease brain tissue, exhibits N-terminal heterogeneity both in vitro and in vivo. To investigate the effects of this N-terminal heterogeneity on the assembly characteristics and biophysical properties of beta-amyloid, we synthesized a series of peptides with progressively shortened N termini (initial residues at positions beta 1, beta 4, beta 8, beta 12, and beta 17) and C termini extending to residue beta 40 or beta 42. We report that peptides with N-terminal deletions exhibit enhanced peptide aggregation relative to full-length species, as quantitatively assessed by sedimentation analyses. Overall, sedimentation levels were greater for peptides terminating at residue beta 42 than for those terminating at residue beta 40. To determine if established biophysical features of the full-length protein were maintained in the truncated peptides, structural and bioactive properties of these peptides were examined and compared. Full-length and truncated peptides exhibiting aggregation showed circular dichroism spectra consistent with predominant beta-sheet conformation, fibrillar morphology under transmission electron microscopy, and significant toxicity in cultures of rat hippocampal neurons. These data demonstrate that N-terminal deletions enhance aggregation of beta-amyloid into neurotoxic, beta-sheet fibrils and suggest that such peptides may initiate and/or nucleate the pathological deposition of beta-amyloid.

Publication types

  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Alzheimer Disease / metabolism
  • Amyloid beta-Peptides / chemistry*
  • Amyloid beta-Peptides / toxicity
  • Amyloid beta-Peptides / ultrastructure
  • Animals
  • Brain / metabolism
  • Cells, Cultured
  • Circular Dichroism
  • Embryo, Mammalian
  • Hippocampus / cytology
  • Humans
  • Indicators and Reagents
  • Microscopy, Electron
  • Neurons / cytology
  • Neurons / drug effects
  • Neurotoxins / chemistry
  • Neurotoxins / toxicity
  • Peptide Fragments / chemical synthesis
  • Peptide Fragments / chemistry*
  • Peptide Fragments / toxicity
  • Protein Structure, Secondary*
  • Rats
  • Rats, Sprague-Dawley

Substances

  • Amyloid beta-Peptides
  • Indicators and Reagents
  • Neurotoxins
  • Peptide Fragments