dc.creatorValenti, Laura Elisa
dc.creatorBurgos Paci, Maximiliano Alberto
dc.creatorde Pauli, Carlos Primo
dc.creatorGiacomelli, Carla Eugenia
dc.date.accessioned2019-01-04T12:40:46Z
dc.date.accessioned2022-10-15T05:57:36Z
dc.date.available2019-01-04T12:40:46Z
dc.date.available2022-10-15T05:57:36Z
dc.date.created2019-01-04T12:40:46Z
dc.date.issued2011-03
dc.identifierValenti, Laura Elisa; Burgos Paci, Maximiliano Alberto; de Pauli, Carlos Primo; Giacomelli, Carla Eugenia; Infrared study of trifluoroacetic acid unpurified synthetic peptides in aqueous solution: Trifluoroacetic acid removal and band assignment; Academic Press Inc Elsevier Science; Analytical Biochemistry; 410; 1; 3-2011; 118-123
dc.identifier0003-2697
dc.identifierhttp://hdl.handle.net/11336/67370
dc.identifierCONICET Digital
dc.identifierCONICET
dc.identifier.urihttps://repositorioslatinoamericanos.uchile.cl/handle/2250/4352453
dc.description.abstractSynthetic peptide or protein samples are mostly unpurified with trifluoroacetic acid (TFA) used during the synthesis procedure, which strongly interferes with structure determination by infrared (IR) spectroscopy. The aim of this work was to propose a simple strategy to remove TFA contribution from attenuated total reflection (ATR)-IR spectra of the hexahistidine peptide (His6) in aqueous solution to study the conformation of this synthetic peptide without previous purification. Such a strategy is based on the subtraction mode widely employed to remove water contribution, and it is tested with TFA unpurified histidine as a model system. The subtraction is based on eliminating the strong TFA bands at 1147 and 1200 cm-1 by applying a scaling factor (as in buffer correction). The proposed modes represent excellent strategies that do not modify spectral features, and they provide reliable routines to obtain the synthetic peptide spectrum without TFA contribution. The conformational information from the corrected spectra at different pH values is deduced from semiempirical calculated IR spectra of different His6 conformers. The spectral features and the band positions of the corrected spectrum suggest that the peptide molecules mainly adopt an intermolecular β-sheet structure.
dc.languageeng
dc.publisherAcademic Press Inc Elsevier Science
dc.relationinfo:eu-repo/semantics/altIdentifier/url/https://www.sciencedirect.com/science/article/pii/S0003269710007190
dc.relationinfo:eu-repo/semantics/altIdentifier/doi/https://doi.org/10.1016/j.ab.2010.11.006
dc.rightshttps://creativecommons.org/licenses/by-nc-sa/2.5/ar/
dc.rightsinfo:eu-repo/semantics/restrictedAccess
dc.subjectAtr-Ir
dc.subjectBand Assignment
dc.subjectHexahistidine
dc.subjectSemiempirical Calculations
dc.subjectTfa Subtraction
dc.titleInfrared study of trifluoroacetic acid unpurified synthetic peptides in aqueous solution: Trifluoroacetic acid removal and band assignment
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:ar-repo/semantics/artículo
dc.typeinfo:eu-repo/semantics/publishedVersion


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