Article ID Journal Published Year Pages File Type
5622646 Alzheimer's & Dementia 2015 20 Pages PDF
Abstract

IntroductionMuch knowledge about amyloid β (Aβ) aggregation and toxicity has been acquired using synthetic peptides and mouse models, whereas less is known about soluble Aβ in human brain.MethodsWe analyzed aqueous extracts from multiple AD brains using an array of techniques.ResultsBrains can contain at least four different Aβ assembly forms including: (i) monomers, (ii) a ∼7kDa Aβ species, and larger species (iii) from ∼30-150 kDa, and (iv) >160 kDa. High molecular weight species are by far the most prevalent and appear to be built from ∼7 kDa Aβ species. The ∼7 kDa Aβ species resist denaturation by chaotropic agents and have a higher Aβ42/Aβ40 ratio than monomers, and are unreactive with antibodies to Asp1 of Ab or APP residues N-terminal of Asp1.DiscussionFurther analysis of brain-derived ∼7 kDa Aβ species, the mechanism by which they assemble and the structures they form should reveal therapeutic and diagnostic opportunities.

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