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dc.contributor.authorTasiopoulos, A. J.en
dc.contributor.authorTolis, E. J.en
dc.contributor.authorTsangaris, J. M.en
dc.contributor.authorEvangelou, A.en
dc.contributor.authorWoollins, J. D.en
dc.contributor.authorSlawin, A. M. Z.en
dc.contributor.authorPessoa, J. C.en
dc.contributor.authorCorreia, I.en
dc.contributor.authorKabanos, T. A.en
dc.date.accessioned2015-11-24T16:41:57Z-
dc.date.available2015-11-24T16:41:57Z-
dc.identifier.issn0949-8257-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8494-
dc.rightsDefault Licence-
dc.subjectvanadiumen
dc.subjectpeptidesen
dc.subjectcircular dichroismen
dc.subjectelectron paramagnetic resonanceen
dc.subjectsulfhydryl-containing pseudopeptidesen
dc.subjectsynthetic analogsen
dc.subjectcrystal-structureen
dc.subjectcomplexesen
dc.subjectchemistryen
dc.subjectpeptidesen
dc.subjectnitrogenaseen
dc.subjectbindingen
dc.subjectligandsen
dc.subjectepren
dc.titleModel investigations for vanadium-protein interactions: vanadium(III) compounds with dipeptides and their oxovanadium(IV) analoguesen
heal.typejournalArticle-
heal.type.enJournal articleen
heal.type.elΆρθρο Περιοδικούel
heal.identifier.primaryDOI 10.1007/s00775-001-0308-0-
heal.identifier.secondary<Go to ISI>://000174957800002-
heal.identifier.secondaryhttp://www.springerlink.com/content/te6xektmf6hyg4j8/fulltext.pdf-
heal.languageen-
heal.accesscampus-
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.publicationDate2002-
heal.abstractThe reaction of VCl3 with 1,10-phenanthroline and a series of dipeptides (H(2)dip), having aliphatic as well as aromatic side chains, in methyl alcohol and in the presence of triethylamine affords vanadium(III) compounds of the general formula [V-III(dip)(MeOH) (phen)]Cl. Aerial oxidation/hydrolysis of the vanadium(III) species gives their oxovanadium(IV) analogues of the general formula [(VO)-O-IV(dip)(phen)] X-ray crystallographic characterization of the [(VO)-O-IV(dip)(phen)] compounds (where dip(2-) = Gly-L-Ala, Gly-L-Val and Gly-L-Phe) revealed that the vanadium atom possesses a severely distorted octahedral coordination and is ligated to a tridentate dip(2-) ligand at the N-amine atom, the deprotonated N-peptide atom and one of the O-carboxylate atoms, as well as an oxo group and two phenanthroline nitrogen atoms. Circular dichroism characterization of the V-III/(VO2+)-O-IV-dipeptide compounds revealed a strong signal for the (VO2+)-O-IV species in the visible range of the spectrum, with a characteristic pattern which may be exploited to identify the N-am, N-pep and O-car ligation of a peptide or a protein to (VO2+)-O-IV center, and a weak Cotton effect of opposite sign to their vanadium(III) analogues. The visible spectra of the V-III-dipeptide compounds revealed two d-d bands with high intensity, thus indicating that the covalency of the metal-donor atoms is significant, i.e. the vanadium d orbitals are significantly mixed with the ligand orbitals, and this is confirmed by the low values of their Racah B parameters. The high-intensity band of the (VO2+)-O-IV-dipeptide compounds at similar to460 nm implies also a strong covalency of the metal with the equatorial donor atoms and this was supported by the EPR spectra of these compounds. Moreover, the V-III/(VO2+)-O-IV-dipeptide complexes were characterized by EPR and IR spectroscopies as well as conductivity and magnetic susceptibility measurements.en
heal.publisherSpringer Verlag (Germany)en
heal.journalNameJournal of Biological Inorganic Chemistryen
heal.journalTypepeer reviewed-
heal.fullTextAvailabilityTRUE-
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