1. Academic Validation
  2. Amyloidogenicity and toxicity of the reverse and scrambled variants of amyloid-β 1-42

Amyloidogenicity and toxicity of the reverse and scrambled variants of amyloid-β 1-42

  • FEBS Lett. 2017 Mar;591(5):822-830. doi: 10.1002/1873-3468.12590.
Devkee M Vadukul 1 Oyinkansola Gbajumo 1 Karen E Marshall 1 Louise C Serpell 1
Affiliations

Affiliation

  • 1 School of Life Sciences, University of Sussex, Falmer, UK.
Abstract

β-amyloid 1-42 (Aβ1-42) is a self-assembling peptide that goes through many conformational and morphological changes before forming the fibrils that are deposited in extracellular plaques characteristic of Alzheimer's disease. The link between Aβ1-42 structure and toxicity is of major interest, in particular, the neurotoxic potential of oligomeric species. Many studies utilise reversed (Aβ42-1) and scrambled (AβS) forms of Amyloid-β as control peptides. Here, using circular dichroism, thioflavin T fluorescence and transmission electron microscopy, we reveal that both control peptides self-assemble to form fibres within 24 h. However, oligomeric Aβ reduces cell survival of hippocampal neurons, while Aβ42-1 and Aβs have reduced effect on cellular health, which may arise from their ability to assemble rapidly to form protofibrils and fibrils.

Keywords

Alzheimer's disease; amyloid fibril; amyloid-β, control; cytotoxicity; self-assembly.

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