Aberrant protein oligomerization is an important pathogenetic process in vivo. In Alzheimer's disease, the amyloid β-protein forms neurotoxic oligomers. The predominant in vivo Aβ alloforms, Aβ40 and Aβ42, have distinct oligomerization pathways. Aβ42 monomers oligomerize into pentamer/hexamer units which self-associate to form larger oligomers. Aβ40 does not form these paranuclei, a fact which may explain the particularly strong linkage of Aβ42 with AD. Here, we sought to determine the structura…
Read moreAberrant protein oligomerization is an important pathogenetic process in vivo. In Alzheimer's disease, the amyloid β-protein forms neurotoxic oligomers. The predominant in vivo Aβ alloforms, Aβ40 and Aβ42, have distinct oligomerization pathways. Aβ42 monomers oligomerize into pentamer/hexamer units which self-associate to form larger oligomers. Aβ40 does not form these paranuclei, a fact which may explain the particularly strong linkage of Aβ42 with AD. Here, we sought to determine the structural elements controlling paranucleus formation as a first step toward the development of strategies for treating AD. Because oxidation of Met35 is associated with altered Aβ assembly, we examined the role of Met35 in controlling Aβ oligomerization. Oxidation of Met35 in Aβ42 blocked paranucleus formation and produced oligomers indistinguishable in size and morphology from those produced by Aβ40. Systematic structural alterations of the Cγ 35-substituent group revealed that its electronic nature, rather than its size, was the factor controlling oligomerization pathway choice. Preventing assembly of toxic Aβ42 paranuclei through selective oxidation of Met35 thus represents a potential therapeutic approach for AD.
