Interaction of Lambda- and Delta-[Ru(bpy)(2)(pbmz)](PF6)(2) with the oligonucleotide duplex d(CGCGAATTCGCG)(2)

dc.contributor.authorPapakyriakou, A.en
dc.contributor.authorMalandrinos, G.en
dc.contributor.authorGaroufis, A.en
dc.date.accessioned2015-11-24T16:40:15Z
dc.date.available2015-11-24T16:40:15Z
dc.identifier.issn0162-0134-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/8251
dc.rightsDefault Licence-
dc.subjectrutheniumen
dc.subjectoligonucleotideen
dc.subjectnmr spectroscopyen
dc.subjectgroove bindersen
dc.subjectbenzimidazoleen
dc.subjectruthenium(ii) complexesen
dc.subjectphotophysical propertiesen
dc.subjectstereospecific bindingen
dc.subjectmolecular-dynamicsen
dc.subjectnmr-spectroscopyen
dc.subjectgroove bindingen
dc.subjectmajor grooveen
dc.subjectDNA-bindingen
dc.subjectdichroismen
dc.subject2,2'-bipyridineen
dc.titleInteraction of Lambda- and Delta-[Ru(bpy)(2)(pbmz)](PF6)(2) with the oligonucleotide duplex d(CGCGAATTCGCG)(2)en
heal.abstractThe interaction of the enantiomeric complexes Lambda- and Delta-[Ru(bpy)(2)(pbmz)](PF6)(2) (bpy = 2,2'-bipyridine, pbmz = 2-(2'-pyridyl)benzimidazole) with the DNA duplex d(CGCGAATTCGCG)(2) was investigated by means of 2D NMR techniques. The synthesis of the enantiomers was based on the optically pure complexes Lambda- and Delta-[Ru(bPY)(2)(PY)(2)](2+) and were characterized by CD and NMR spectroscopy. NMR data indicate that both enantiomers bind weakly to the oligonucleotide, approaching from the minor groove at the centre of the helix. The perturbation of the B-DNA conformation is minor with an apparent absence of enantio selectivity. Molecular modelling calculations in conjunction with the NOE data support the suggestion that more than one binding modes are present. The imidazole amine group of the pbmz ligand is probably hydrogen bonded to the DNA phosphodiesteric backbone at the AATT step, and this may provide an explanation for the diminished enantioselectivity observed. (c) 2006 Elsevier Inc. All rights reserved.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1016/j.jinorgbio.2006.07.008-
heal.identifier.secondary<Go to ISI>://000242274800016-
heal.identifier.secondaryhttp://ac.els-cdn.com/S0162013406002133/1-s2.0-S0162013406002133-main.pdf?_tid=22113c055145d88d1950efb41d3b909d&acdnat=1333034647_da14f17ca30ad60aaef72bcde54cf948-
heal.journalNameJ Inorg Biochemen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2006-
heal.publisherElsevieren
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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