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• W2889019675 abstract "Since the introduction of acetyl cholinesterase inhibitors as the first approved drugs by the US Food and Drug Administration for Alzheimer’s disease (AD) in clinics, less than satisfactory success in the design of anti-AD agents has impelled the scientists to also focus toward inhibition of Aβ aggregation. Considering the specific binding of fragments for their parent peptide, herein, we synthesized more than 40 new peptides based on a C-terminus tetrapeptide fragment of Aβ1–42. Initial screening by MTT cell viability assay and supportive results by ThT fluorescence assay led us to identify a tetrapeptide showing complete inhibition for Aβ1–42 aggregation. Peptide 20 displayed 100% cell viability at 20 μM concentration, while at lower concentrations of 10 and 2 μM 76.6 and 70% of cells were viable. Peptide 20 was found to restrict the conformational transition of Aβ1–42 peptide toward β-sheet structure. Inhibitory activity of tetrapeptide 20 was further evidenced by the absence of Aβ1–42 aggregates in electron microscopy. Peptide 20 and other significantly active tetrapeptide analogues could prove imperative in the future design of anti-AD agents." @default.
• W2889019675 created "2018-09-07" @default.
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• W2889019675 date "2018-08-28" @default.
• W2889019675 modified "2023-10-18" @default.
• W2889019675 title "C-Terminal Fragment, Aβ_39–42-Based Tetrapeptides Mitigates Amyloid-β Aggregation-Induced Toxicity" @default.
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• W2889019675 doi "https://doi.org/10.1021/acsomega.8b01522" @default.
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