posted on 2016-08-09, 00:00authored byGhiam Yamin, Giovanni Coppola, David B. Teplow
A key
pathogenic agent in Alzheimer’s disease (AD) is the
amyloid β-protein (Aβ), which self-assembles into a variety
of neurotoxic structures. Establishing structure–activity relationships
for these assemblies, which is critical for proper therapeutic target
identification and design, requires aggregation and neurotoxicity
experiments that are properly controlled with respect to the Aβ
peptide itself. “Reverse” Aβ or non-Aβ peptides
suffer from the fact that their biophysical properties are too similar
or dissimilar, respectively, to those of native Aβ for them
to be appropriate controls. For this reason, we used simple protein
design principles to create scrambled Aβ peptides predicted
to behave distinctly from native Aβ. We showed that our prediction
was true by monitoring secondary structure dynamics with thioflavin
T fluorescence and circular dichroism spectroscopy, determining oligomer
size distributions, and assaying neurotoxic activity. We then demonstrated
the utility of the scrambled Aβ peptides by using them to control
experiments examining the effects of Aβ monomers, dimers, higher-order
oligomers, and fibrils on gene expression in primary rat hippocampal
neurons. Significant changes in gene expression were observed for
all peptide assemblies, but fibrils induced the largest changes. Weighted
gene co-expression network analysis revealed two predominant gene
modules related to Aβ treatment. Many genes within these modules
were associated with inflammatory signaling pathways.