A Beta 42-Oligomer Interacting Peptide (Aip) Neutralizes Toxic Amyloid-Beta 42 Species And Protects Synaptic Structure And Function

The amyloid-beta 42 (A beta 42) peptide is believed to be the main culprit in the pathogenesis of Alzheimer disease (AD), impairing synaptic function and initiating neuronal degeneration. Soluble A beta 42 oligomers are highly toxic and contribute to progressive neuronal dysfunction, loss of synaptic spine density, and affect long-term potentiation (LTP). We have characterized a short, L-amino acid A beta-oligomer Interacting Peptide (AIP) that targets a relatively well-defined population of low-n A beta 42 oligomers, rather than simply inhibiting the aggregation of A beta monomers into oligomers. Our data show that AIP diminishes the loss of A beta 42-induced synaptic spine density and rescues LTP in organotypic hippocampal slice cultures. Notably, the AIP enantiomer (comprised of D-amino acids) attenuated the rough-eye phenotype in a transgenic A beta 42 fly model and significantly improved the function of photoreceptors of these flies in electroretinography tests. Overall, our results indicate that specifically "trapping" low-n oligomers provides a novel strategy for toxic A beta 42-oligomer recognition and removal.