A resorcinarene for inhibition of Aβ fibrillation. Issue 3 (28th November 2016)

• Record Type: Journal Article
• Authors: Han, Xu; Park, Jiyong; Wu, Wei; Malagon, Andres; Wang, Lingyu; Vargas, Edgar; Wikramanayake, Athula; Houk, K. N.; Leblanc, Roger M.
• Is Part Of: Chemical science. Volume 8:Issue 3(2017)
• Page Start: 2003
• Page End: 2009
• Publication Date: 2016-11-28
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c6sc04854d
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : Low toxic resorcinarene can effectively inhibit Aβ fibrillation and delay the formation of toxic Aβ 42 species. Abstract : Amyloid-β peptides (Aβ) fibrillation is the hallmark of Alzheimer's disease (AD). However, it has been challenging to discover potent agents in order to inhibit Aβ fibrillation. Herein, we demonstrated the effect of resorcinarene on inhibiting Aβ fibrillation in vitro via experimental and computational methods. Aβ were incubated with different concentrations of resorcinarene so as to monitor the kinetics by using thioflavin T binding assay. The results, which were further confirmed by far-UV CD spectroscopy and atomic force microscopy, strongly indicated that the higher concentration of resorcinarene, the more effective the inhibition of Aβ fibrillation. A cytotoxicity study showed that when sea urchin embryos were exposed to the resorcinarene, the majority survived due to the resorcinarene low toxicity. In addition, when the resorcinarene was added, the formation of toxic Aβ 42 species was delayed. Computational studies of Aβ fibrillation, including docking simulations and MD simulations, illustrated that the interaction between inhibitor resorcinarene and Aβ is driven by the non-polar interactions. These studies display a novel strategy for the exploration of promising antiamyloiddogenic agents for AD treatments.