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Proteins multi-funnel energy landscape and misfolding diseases

dc.contributor.authorCruzeiro, Leonor
dc.date.accessioned2014-02-28T20:36:20Z
dc.date.available2014-02-28T20:36:20Z
dc.date.issued2008
dc.date.updated2014-02-27T16:44:03Z
dc.description.abstractThe problem of how a given a-amino acid sequence, in cells, most of the times, assumes the native structure, is a fundamental problem in Biology, known as the protein folding problem. Here, evidence is presented that suggests that the same a-amino acid sequence can assume several, very different, structures that have the same Gibbs energy as the native structure, in the same thermodynamic conditions. These results lend support to a multi-funnel Gibbs energy landscape for proteins in which Anfinsen’s thermodynamic hypothesis alone cannot explain protein folding. How then do proteins fold? In a multi-funnel picture, transient deterministic forces are needed to select the native funnel from all other funnels that the protein can potentially fall into. The suggestion here is that such transient, deterministic forces arise from specific vibrational excited states (VES) that constitute the first step in protein folding and function (the VES hypothesis). An application of the VES hypothesis to calculate the energy absorbed, from water molecules, by a protein a-helix with extensive glutamine (gln) repeats is made, which can explain the structural instability of these proteins and their association with many misfolding diseases.por
dc.identifier.citationCruzeiro, L.Proteins multi-funnel energy landscape and misfolding diseases, Journal of Physical Organic Chemistry, 21, 7-8, 549-554, 2008.por
dc.identifier.doihttp://dx.doi.org/10.1002/poc.1315
dc.identifier.issn0894-3230
dc.identifier.otherAUT: LHA01632;
dc.identifier.urihttp://hdl.handle.net/10400.1/3543
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherWileypor
dc.relation.publisherversionhttp://onlinelibrary.wiley.com/doi/10.1002/poc.1315/pdfpor
dc.subjectEnergy landscapepor
dc.subjectProtein foldingpor
dc.subjectVES hypothesispor
dc.subjectDavydov/Scott modelpor
dc.titleProteins multi-funnel energy landscape and misfolding diseasespor
dc.typejournal article
dspace.entity.typePublication
oaire.citation.endPage554por
oaire.citation.issue7-8
oaire.citation.startPage549por
oaire.citation.titleJournal of Physical Organic Chemistrypor
oaire.citation.volume21por
rcaap.rightsrestrictedAccesspor
rcaap.typearticlepor

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