Mostrar el registro sencillo del ítem

dc.contributor.author
Castelletto, V.  
dc.contributor.author
Ryumin, P.  
dc.contributor.author
Cramer, R.  
dc.contributor.author
Hamley, I.W.  
dc.contributor.author
Taylor, M.  
dc.contributor.author
Allsop, D.  
dc.contributor.author
Reza, M.  
dc.contributor.author
Ruokolainen, J.  
dc.contributor.author
Arnold, T.  
dc.contributor.author
Hermida Merino, D.  
dc.contributor.author
Garcia, Corina Ileana  
dc.contributor.author
Leal, Maria Celeste  
dc.contributor.author
Castaño, Eduardo Miguel  
dc.date.available
2019-12-26T17:05:58Z  
dc.date.issued
2017-03  
dc.identifier.citation
Castelletto, V.; Ryumin, P.; Cramer, R.; Hamley, I.W.; Taylor, M.; et al.; Self-assembly and anti-amyloid cytotoxicity activity of amyloid beta peptide derivatives; Nature Publishing Group; Scientific Reports; 7; 3-2017  
dc.identifier.issn
2045-2322  
dc.identifier.uri
http://hdl.handle.net/11336/92942  
dc.description.abstract
The self-assembly of two derivatives of KLVFF, a fragment Aβ(16-20) of the amyloid beta (Aβ) peptide, is investigated and recovery of viability of neuroblastoma cells exposed to Aβ (1-42) is observed at sub-stoichiometric peptide concentrations. Fluorescence assays show that NH 2 -KLVFF-CONH 2 undergoes hydrophobic collapse and amyloid formation at the same critical aggregation concentration (cac). In contrast, NH 2 -K(Boc)LVFF-CONH 2 undergoes hydrophobic collapse at a low concentration, followed by amyloid formation at a higher cac. These findings are supported by the β-sheet features observed by FTIR. Electrospray ionization mass spectrometry indicates that NH 2 -K(Boc)LVFF-CONH 2 forms a significant population of oligomeric species above the cac. Cryo-TEM, used together with SAXS to determine fibril dimensions, shows that the length and degree of twisting of peptide fibrils seem to be influenced by the net peptide charge. Grazing incidence X-ray scattering from thin peptide films shows features of β-sheet ordering for both peptides, along with evidence for lamellar ordering of NH 2 -KLVFF-CONH 2. This work provides a comprehensive picture of the aggregation properties of these two KLVFF derivatives and shows their utility, in unaggregated form, in restoring the viability of neuroblastoma cells against Aβ-induced toxicity.  
dc.format
application/pdf  
dc.language.iso
eng  
dc.publisher
Nature Publishing Group  
dc.rights
info:eu-repo/semantics/openAccess  
dc.rights.uri
https://creativecommons.org/licenses/by-nc-sa/2.5/ar/  
dc.subject
Alzheimer Diseade  
dc.subject
Amyloid Beta  
dc.subject
Neurodegeneration  
dc.subject
Amyloid Beta  
dc.subject.classification
Neurociencias  
dc.subject.classification
Medicina Básica  
dc.subject.classification
CIENCIAS MÉDICAS Y DE LA SALUD  
dc.title
Self-assembly and anti-amyloid cytotoxicity activity of amyloid beta peptide derivatives  
dc.type
info:eu-repo/semantics/article  
dc.type
info:ar-repo/semantics/artículo  
dc.type
info:eu-repo/semantics/publishedVersion  
dc.date.updated
2019-05-10T14:12:43Z  
dc.journal.volume
7  
dc.journal.pais
Reino Unido  
dc.description.fil
Fil: Castelletto, V.. University of Reading; Reino Unido  
dc.description.fil
Fil: Ryumin, P.. University of Reading; Reino Unido  
dc.description.fil
Fil: Cramer, R.. University of Reading; Reino Unido  
dc.description.fil
Fil: Hamley, I.W.. University of Reading; Reino Unido  
dc.description.fil
Fil: Taylor, M.. University of Lancaster; Reino Unido  
dc.description.fil
Fil: Allsop, D.. University of Lancaster; Reino Unido  
dc.description.fil
Fil: Reza, M.. Aalto University; Finlandia  
dc.description.fil
Fil: Ruokolainen, J.. Aalto University; Finlandia  
dc.description.fil
Fil: Arnold, T.. Diamond Light Source Ltd.,Harwell Science and Innovation Campus; Reino Unido  
dc.description.fil
Fil: Hermida Merino, D.. European Synchrotron Radiation Facility; Francia  
dc.description.fil
Fil: Garcia, Corina Ileana. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina  
dc.description.fil
Fil: Leal, Maria Celeste. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina  
dc.description.fil
Fil: Castaño, Eduardo Miguel. Consejo Nacional de Investigaciones Científicas y Técnicas. Oficina de Coordinación Administrativa Parque Centenario. Instituto de Investigaciones Bioquímicas de Buenos Aires. Fundación Instituto Leloir. Instituto de Investigaciones Bioquímicas de Buenos Aires; Argentina  
dc.journal.title
Scientific Reports  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/url/http://www.nature.com/articles/srep43637  
dc.relation.alternativeid
info:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1038/srep43637