Journal
PEERJ
Volume 1, Issue -, Pages -Publisher
PEERJ INC
DOI: 10.7717/peerj.73
Keywords
Amyloid; Hexafluoroisopropanol; Ammonium Hydroxide; Aggregation; A beta; A beta toxicity; Oligomers
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Funding
- CSIRO, a NHMRC program grant
- Victorian government's operational support program
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Alzheimer's disease is the leading cause of dementia in the elderly. Pathologically it is characterized by the presence of amyloid plaques and neuronal loss within the brain tissue of affected individuals. It is now widely hypothesised that fibrillar structures represent an inert structure. Biophysical and toxicity assays attempting to characterize the formation of both the fibrillar and the intermediate oligomeric structures of A beta typically involves preparing samples which are largely monomeric; the most common method by which this is achieved is to use the fluorinated organic solvent 1,1,1,3,3,3-hexafluoro-2-propanol (HFIP). Recent evidence has suggested that this method is not 100% effective in producing an aggregate free solution. We show, using dynamic light scattering, size exclusion chromatography and small angle X-ray scattering that this is indeed the case, with HFIP pretreated A beta peptide solutions displaying an increased proportion of oligomeric and aggregated material and an increased propensity to aggregate. Furthermore we show that an alternative technique, involving treatment with strong alkali results in a much more homogenous solution that is largely monomeric. These techniques for solubilising and controlling the oligomeric state of A beta are valuable starting points for future biophysical and toxicity assays.
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