| Literature DB >> 28004889 |
Hyuck Jin Lee1, Kyle J Korshavn2, Younwoo Nam3, Juhye Kang3, Thomas J Paul4, Richard A Kerr2, Il Seung Youn3, Mehmet Ozbil4, Kwang S Kim3, Brandon T Ruotolo2, Rajeev Prabhakar4, Ayyalusamy Ramamoorthy2,5, Mi Hee Lim3.
Abstract
To elucidate the involvement of individual and inter-related pathological factors [i.e., amyloid-β (Aβ), metals, and oxidative stress] in the pathogenesis of Alzheimer's disease (AD), chemical tools have been developed. Characteristics required for such tool construction, however, have not been clearly identified; thus, the optimization of available tools or new design has been limited. Here, key structural properties and mechanisms that can determine tools' regulatory reactivities with multiple pathogenic features found in AD are reported. A series of small molecules was built up through rational structural selection and variations onto the framework of a tool useful for in vitro and in vivo metal-Aβ investigation. Variations include: (i) location and number of an Aβ interacting moiety; (ii) metal binding site; and (iii) denticity and structural flexibility. Detailed biochemical, biophysical, and computational studies were able to provide a foundation of how to originate molecular formulas to devise chemical tools capable of controlling the reactivities of various pathological components through distinct mechanisms. Overall, this multidisciplinary investigation illustrates a structure-mechanism-based strategy of tool invention for such a complicated brain disease.Entities:
Keywords: amyloid beta-peptides; chemical tools; metal ions; oxidative stress; structure-activity relationships
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Year: 2017 PMID: 28004889 PMCID: PMC5826595 DOI: 10.1002/chem.201605401
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236