Abstract
There are two different prion conformations: (1) the cellular natural (PrPC) and (2) the scrapie (PrPSc), an infectious form that tends to aggregate under specific conditions. PrPC and PrPSc are widely different regarding secondary and tertiary structures. PrPSc contains more and longer β-strands compared to PrPC. The lack of solved PrPSc structures precludes a proper understanding of the mechanisms related to the transition between cellular and scrapie forms, as well as the aggregation process. In order to investigate the conformational transition between PrPC and PrPSc, we applied MDeNM (molecular dynamics with excited normal modes), an enhanced sampling simulation technique that has been recently developed to probe large structural changes. These simulations yielded new structural rearrangements of the cellular prion that would have been difficult to obtain with standard MD simulations. We observed an increase in β-sheet formation under low pH (≤ 4) and upon oligomerization, whose relevance was discussed on the basis of the energy landscape theory for protein folding. The characterization of intermediate structures corresponding to transition states allowed us to propose a conversion model from the cellular to the scrapie prion, which possibly ignites the fibril formation. This model can assist the design of new drugs to prevent neurological disorders related to the prion aggregation mechanism.
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Acknowledgements
ANL thanks UFABC and the Brazilian Agencies FAPESP and CAPES (CAPES Scholarship—Proc. nº 7121/12-1). RJO thanks the Brazilian Agencies FAPEMIG, CAPES and CNPq and the facilities GridUnesp and Prof. V.B.P. Leite’s cluster (Fapesp Grant 2011/17658-3) for the computational resources. ANL thanks Patricia Cassiolato Tufanetto for helping to write the manuscript.
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Lima, A.N., de Oliveira, R.J., Braz, A.S.K. et al. Effects of pH and aggregation in the human prion conversion into scrapie form: a study using molecular dynamics with excited normal modes. Eur Biophys J 47, 583–590 (2018). https://doi.org/10.1007/s00249-018-1292-4
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DOI: https://doi.org/10.1007/s00249-018-1292-4