Biophysical and morphological studies on the dual interaction of non-octarepeat prion protein peptides with copper and nucleic acids


Conversion of prion protein (PrP) to an altered conformer, the scrapie PrP (PrPSc), is a critical step in the development of transmissible spongiform encephalopathies. Both Cu(II) and nucleic acid molecules have been implicated in this conversion. Full-length PrP can bind up to six copper ions; four Cu(II) binding sites are located in the octarepeat domain (residues 60–91), and His-96 and His-111 coordinate two additional copper ions. Experimental evidence shows that PrP binds different molecules, resulting in diverse cellular signaling events. However, there is little information about the interaction of macromolecular ligands with Cu(II)-bound PrP. Both RNA and DNA sequences can bind PrP, and this interaction results in reciprocal conformational changes. Here, we investigated the interaction of Cu(II) and nucleic acids with amyloidogenic non-octarepeat PrP peptide models (comprising human PrP residues 106–126 and hamster PrP residues 109–149) that retain His-111 as the copper-anchoring residue. The effect of Cu(II) and DNA or RNA sequences in the aggregation, conformation, and toxicity of PrP domains was investigated at low and neutral pH. Circular dichroism and EPR spectroscopy data indicate that interaction of the PrP peptides with Cu(II) and DNA occurs at pH 7. This dual interaction induces conformational changes in the peptides, modulating their aggregation, and affecting the morphology of the aggregated species, resulting in different cytotoxic effects. These results provide new insights into the role of Cu(II) and nucleic acid sequences in the structural conversion and aggregation of PrP, which are both critical events related to prion pathogenesis.

DOI: 10.1007/s00775-014-1115-8

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@article{Chaves2014BiophysicalAM, title={Biophysical and morphological studies on the dual interaction of non-octarepeat prion protein peptides with copper and nucleic acids}, author={Juliana A. P. Chaves and Carolina S{\'a}nchez-L{\'o}pez and Mariana P. B. Gomes and Th{\'a}yna Sisnande and Bruno Macedo and Vanessa End de Oliveira and Carolina A. C. Braga and Luciana Pereira Rangel and Jerson L Silva and Liliana Quintanar and Yraima Cordeiro}, journal={JBIC Journal of Biological Inorganic Chemistry}, year={2014}, volume={19}, pages={839-851} }