Solid-phase synthesis, characterization and DNA binding properties of the first chloro(polypyridyl)ruthenium conjugated peptide complex

dc.contributor.authorKaridi, K.en
dc.contributor.authorGaroufis, A.en
dc.contributor.authorHadjiliadis, N.en
dc.contributor.authorReedijk, J.en
dc.date.accessioned2015-11-24T16:47:30Z
dc.date.available2015-11-24T16:47:30Z
dc.identifier.issn1477-9226-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9194
dc.rightsDefault Licence-
dc.subjectphotoinduced electron-transferen
dc.subjectnmren
dc.subjectproteinen
dc.subjectoxidationen
dc.subjectmetallointercalatoren
dc.subjectspectroscopyen
dc.subjectcellsen
dc.titleSolid-phase synthesis, characterization and DNA binding properties of the first chloro(polypyridyl)ruthenium conjugated peptide complexen
heal.abstractA general method for the synthesis of chloro(polypyridyl) ruthenium conjugated peptide complexes via a solid-phase strategy is described. The method is applied to synthesize two positional isomers of the complex [Ru(terpy) (4-CO2H-4 - Mebpy-Gly-L-His-L-LysCONH(2)) Cl] (PF6). Even though the separation of the isomers was only partially achieved chromatographically, the isomers were unambiguously assigned by NMR spectroscopy. The interactions of the complex [Ru(terpy) (4-CO2H-4'-Mebpy-Gly-L-His-L-LysCONH(2)) Cl] (PF6) with CT-DNA and plasmid DNA, have been studied with various spectroscopic techniques, showing that (i) the complexes coordinatively bind to DNA preferring the bases guanine and cytosine over the bases thymine and adenine after hydrolysis of the coordinated chloride, (ii) electrostatic interactions between the complex cation and the polyanionic DNA chain assist this binding (iii) only in the case of one isomer the peptide does interact further with DNA as evidenced from P-31 NMR spectroscopy, (iv) DNA unwinding occurs in all cases with high binding ratio (Ru/base) values (r > 0.3).en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDoi 10.1039/B410402a-
heal.identifier.secondary<Go to ISI>://000226844900014-
heal.identifier.secondaryhttp://pubs.rsc.org/en/content/articlepdf/2005/dt/b410402a-
heal.journalNameDalton Transactionsen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2005-
heal.publisherRoyal Society of Chemistryen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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