Catalytic Cross Talk Between Key Peptide Fragments That Couple Alzheimer'S Disease With Amyotrophic Lateral Sclerosis

Protein aggregation is a common feature in prominent neurodegenerative diseases, usually thought to be due to the assembly of a single peptide or protein. Recent studies have challenged this notion and suggested several proteins may be involved in promoting and amplifying disease. For example, the TDP-43 protein associated with Amyotrophic Lateral Sclerosis has been found in the brain along with A beta assemblies associated with Alzheimer's disease, and those patients that show the presence of TDP-43 are 10 times more likely to demonstrate cognitive impairment compared to TDP-43-negative Alzheimer's patients. Here we examine the interactions between the amyloidogenic core of TDP-43, TDP-43(307-319), and a neurotoxic physiologically observed fragment of A beta, A beta(25-35). Utilizing ion mobility mass spectrometry in concert with atomic force microscopy and molecular dynamics simulations, we investigate which oligomers are involved in seeding aggregation across these two different protein systems and gain insight into which structures initiate and result from these interactions. Studies were conducted by mixing A beta(25-35) with the toxic wild type TDP-43(307-319) peptide and with the nontoxic synthetic TDP-43(307-319) mutant, G314V. Our findings identify a strong catalytic effect of TDP-43(307-319) WT monomer in the acceleration of A beta(25-35) aggregation to its toxic cylindrin and beta barrel forms. This observation is unprecedented in both its speed and specificity. Interestingly, the nontoxic G314V mutant of TDP-43(307-319) and dimers or higher order oligomers of WT TDP-43(307-319) do not promote aggregation of A beta(25-35) but rather dissociate preformed toxic higher order oligomers of A beta(25-35). Reasons for these very different behaviors are reported.