Loss of the first β-strand of human prion protein generates an aggregation-competent partially "open" form

Hosszu, L. L. P.; Sangar, D.; Batchelor, M.; Risse, E.; Hounslow, A. M.; Waltho, J. P.; Collinge, J.; Bieschke, J.

doi:10.1101/2022.09.20.508729

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bioRxiv · 10.1101/2022.09.20.508729

Loss of the first β-strand of human prion protein generates an aggregation-competent partially "open" form

Hosszu, L. L. P.·Sangar, D.·Batchelor, M.·Risse, E.·Hounslow, A. M.·Waltho, J. P.·Collinge, J.·Bieschke, J.

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Abstract

Prion diseases, a group of incurable, lethal neurodegenerative disorders of mammals including humans, are caused by prions, assemblies of misfolded host prion protein (PrP). The pathway of PrP misfolding is still unclear, though previous data indicate the presence of a structural core in cellular PrP (PrPC), whose cooperative unfolding presents a substantial energy barrier on the path to prion formation. PrP is a GPI-anchored membrane protein, and a number of studies suggest that membrane interactions play an important role in the conversion of PrPC to its disease-associated form, including a transmembrane form of PrP in which a highly conserved region (residues 110 - 136) spans the ER membrane. Insertion of this region results in the detachment of the PrPC first {beta}-strand from the structural core. The effect of this removal on the structure, stability and self-association of the folded domain of PrPC is determined here through a biophysical characterisation of a truncated form of PrPC lacking this region. Whilst markedly destabilised, NMR chemical shifts show that the truncated protein exhibits tertiary structure characteristic of a fully folded protein and retains its native secondary structure elements, including the second strand of the PrP {beta}-sheet, but with altered conformational flexibility in the {beta}2-2 loop and first -helix. The latter is destabilised relative to the other helical regions of the protein, with markedly increased solvent exposure. This truncated form of PrP fibrilises more readily than the native form of the protein. These data suggest a stepwise mechanism, in which a destabilised "open" form of PrPC may be a key intermediate in the refolding to the fibrillar, pathogenic form of the protein.

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Hosszu, L. L. P., Sangar, D., Batchelor, M., Risse, E., Hounslow, A. M., Waltho, J. P., Collinge, J., Bieschke, J.. 2022-09-21. Loss of the first β-strand of human prion protein generates an aggregation-competent partially "open" form. https://doi.org/10.1101/2022.09.20.508729

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