“Structural characterization of the minimal segment of TDP-43 competent for aggregation”

• Residues 342–366 of TDP-43 can reproduce the complete protein’s cytotoxic effects.
• CD & NMR reveal that peptide composed of residues 342–366 is a random coil.
• Within hours, this peptide spontaneously forms a β-sheet rich aggregate.
• Using MD, we propose a model for the β-rich conformer that seeds aggregation.
• MD shows how mutations and phosphorylation could affect this conformer’s structure.

TDP-43 is a nuclear protein whose abnormal aggregates are implicated in ALS and FTLD. Recently, an Asn/Gln rich C-terminal segment of TDP-43 has been shown to produce aggregation in vitro and reproduce most of the protein’s pathological hallmarks in cells, but little is known about this segment’s structure. Here, CD and 2D heteronuclear NMR spectroscopies provide evidence that peptides corresponding to the wild type and mutated sequences of this segment adopt chiefly disordered conformations that, in the case of the wild type sequence, spontaneously forms a β-sheet rich oligomer. Moreover, MD simulation provides evidence for a structure consisting of two β-strands and a well-defined, yet non-canonical structural element. Furthermore, MD simulations of four pathological mutations (Q343R, N345K, G348V and N352S) occurring in this segment predict that all of them could affect this region’s structure. In particular, the Q343R variant tends to stabilize disordered conformers, N345K permits the formation of longer, more stable β-strands, and G348V tends to shorten and destabilize them. Finally, N352S acts to alter the β-stand register and when S352 is phosphorylated, it induces partial unfolding. Our results provide a better understanding of TDP-43 aggregation process and will be useful to design effectors capable to modulate its progression.

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