کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5622646 | 1406184 | 2015 | 20 صفحه PDF | دانلود رایگان |

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 â¼7kDa Aβ species, and larger species (iii) from â¼30-150 kDa, and (iv) >160 kDa. High molecular weight species are by far the most prevalent and appear to be built from â¼7 kDa Aβ species. The â¼7 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 â¼7 kDa Aβ species, the mechanism by which they assemble and the structures they form should reveal therapeutic and diagnostic opportunities.
Journal: Alzheimer's & Dementia - Volume 11, Issue 11, November 2015, Pages 1286-1305