We recently described multifunctional tools (2a–c) as potent inhibitors of human Cholinesterases (ChEs) also able to modulate events correlated with Ab aggregation. We herein propose a thorough biological and computational analysis aiming at understanding their mechanism of action at the molecular level. Methods: We determined the inhibitory potency of 2a–c on Ab1–42 self-aggregation, the interference of 2a with the toxic Ab oligomeric species and with the postaggregation states by capillary electrophoresis analysis and transmission electron microscopy. The modulation of Ab toxicity was assessed for 2a and 2b on human neuroblastoma cells. The key interactions of 2a with Ab and with the Ab-preformed fibrils were computationally analyzed. 2a–c toxicity profile was also assessed (human hepatocytes and mouse fibroblasts). Results: Our prototypical pluripotent analogue 2a interferes with Ab oligomerization process thus reducing Ab oligomers-mediated toxicity in human neuroblastoma cells. 2a also disrupts preformed fibrils. Computational studies highlighted the bases governing the diversified activities of 2a. Conclusion: Converging analytical, biological, and in silico data explained the mechanism of action of 2a on Ab1–42 oligomers formation and against Ab-preformed fibrils. This evidence, combined with toxicity data, will orient the future design of safer analogues.

Disease modifying anti-Alzheimer's drugs: inhibitors of human cholinesterases interfering with β-amyloid aggregation

COLOMBO, RAFFAELLA;LANNI, CRISTINA;DE LORENZI, ERSILIA;
2014-01-01

Abstract

We recently described multifunctional tools (2a–c) as potent inhibitors of human Cholinesterases (ChEs) also able to modulate events correlated with Ab aggregation. We herein propose a thorough biological and computational analysis aiming at understanding their mechanism of action at the molecular level. Methods: We determined the inhibitory potency of 2a–c on Ab1–42 self-aggregation, the interference of 2a with the toxic Ab oligomeric species and with the postaggregation states by capillary electrophoresis analysis and transmission electron microscopy. The modulation of Ab toxicity was assessed for 2a and 2b on human neuroblastoma cells. The key interactions of 2a with Ab and with the Ab-preformed fibrils were computationally analyzed. 2a–c toxicity profile was also assessed (human hepatocytes and mouse fibroblasts). Results: Our prototypical pluripotent analogue 2a interferes with Ab oligomerization process thus reducing Ab oligomers-mediated toxicity in human neuroblastoma cells. 2a also disrupts preformed fibrils. Computational studies highlighted the bases governing the diversified activities of 2a. Conclusion: Converging analytical, biological, and in silico data explained the mechanism of action of 2a on Ab1–42 oligomers formation and against Ab-preformed fibrils. This evidence, combined with toxicity data, will orient the future design of safer analogues.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/865834
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