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Título: | Combining classical MD and QM calculations to elucidate complex system nucleation: A twisted, three-stranded, parallel β-sheet seeds amyloid fibril conception |
Autor: | Mompeán, Miguel CSIC ORCID ; González, Carlos CSIC ; Lomba, Enrique CSIC ORCID ; Laurents, Douglas V. CSIC ORCID | Fecha de publicación: | 2014 | Citación: | The Journal of Physical Chemistry B 118: 7312- 7316 (2014) | Resumen: | The crystal structure of the Sup35 prion segment, GNNQQNY, revealed precise side chain packing and an extensive H-bond network. However, the conformers and stabilizing interactions involved at nascent amyloid formation are still unclear. Here, long molecular dynamics simulations and quantum mechanical calculations have been utilized to study the conformation and energetics of the initial structure that acts to nucleate further growth. Considering all the plausible intermediates that may act as stepping stones, we find that the initial nucleus is a twisted single-layer, three-stranded parallel β-sheet. H-bonds between β-strands in this twisted sheet, some of which differ from those of the crystal structures nontwisted β-strands, are key for the nucleus formation and stability. High level theoretical calculations of these H-bonds energetics can account for this amyloid-like trimers remarkable stability. The intermeshing of facing sheets to form the dry interface provides less stability and would occur between two three-stranded β-sheets without metastable water nanowires. © 2014 American Chemical Society. | URI: | http://hdl.handle.net/10261/167479 | DOI: | 10.1021/jp503742p | Identificadores: | doi: 10.1021/jp503742p issn: 1520-5207 |
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