Synthesis and characterization of the diastereomers Lambda- and Delta-[Ru(bpy)(2)-(m-bpy-Gly-L-His-L-Lys)]Cl-2 - H-1 NMR studies on their interactions with the deoxynucleotide duplex d[(5 '-CGCGAATTCGCG-3 ')(2)]

dc.contributor.authorMyari, A.en
dc.contributor.authorHadjiliadis, N.en
dc.contributor.authorGaroufis, A.en
dc.date.accessioned2015-11-24T16:48:59Z
dc.date.available2015-11-24T16:48:59Z
dc.identifier.issn1434-1948-
dc.identifier.urihttps://olympias.lib.uoi.gr/jspui/handle/123456789/9408
dc.rightsDefault Licence-
dc.subjectmetallopeptidesen
dc.subjectoligonucleotidesen
dc.subjectrutheniumen
dc.subjectchemical nucleasesen
dc.subjectgrooveen
dc.subjectsequential resonance assignmentsen
dc.subjectDNA-bindingen
dc.subjectnmr-spectroscopyen
dc.subjectminor-grooveen
dc.subjectruthenium(ii) complexesen
dc.subjectnucleic-acidsen
dc.subjectintercalationen
dc.subjectspectraen
dc.subjectpeptideen
dc.subjectoligonucleotidesen
dc.titleSynthesis and characterization of the diastereomers Lambda- and Delta-[Ru(bpy)(2)-(m-bpy-Gly-L-His-L-Lys)]Cl-2 - H-1 NMR studies on their interactions with the deoxynucleotide duplex d[(5 '-CGCGAATTCGCG-3 ')(2)]en
heal.abstractThe synthesis and characterization of the diastereomeric complexes Lambda- and Delta-[Ru(bpy)(2)(m-bpy-GHK)]Cl-2, (GHK = glycine-L-histidine-L-lysine, m-bpy = 4\-methyl-2,2\-bipyridine) as well as their binding properties to the deoxynucleotide duplex d(5'-CGCGAATTCGCG-3')2 studied by means of NMR, ESI-MS and CD spectroscopy, are reported. The ROESY spectrum of Lambda-[Ru(bpy)(2)(m-bpy-GHK)]Cl-2 shows intramolecular cross peaks between the bpy H3 or HT protons and the aromatic H2 and H5 of the histidine imidazole ring, indicating that the peptide adopts an orientation with the imidazole ring close to the bpy ligand, possibly interacting by pi-stacking. The absence of intramolecular cross peaks between the peptide and the bipyridine ligands in the ROESY spectrum of Delta-[Ru(bpy)(2)(m-bpy-GHK)]Cl-2 on the other hand, shows that in this case the peptide is far from the two bpy ligands, having a different orientation from the A isomer. The isomers interact with the oligonucleotide duplex differently. Delta-[Ru(bpy)(2)(m-bpy-GHK)]Cl-2 binds in the oligonucleotide major groove close to the central part of the sequence. A[Ru(bpy)(2)(m-bpy-GHK)]Cl-2 binds, probably non selectively, approaching the helix from the minor groove. It can be concluded that the peptide (GHK) binding leads the rest of the isomer to interact with the oligonucleotide in the case of the A isomer. (C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.en
heal.accesscampus-
heal.fullTextAvailabilityTRUE-
heal.identifier.primaryDOI 10.1002/ejic.200300725-
heal.identifier.secondary<Go to ISI>://000220797100009-
heal.identifier.secondaryhttp://onlinelibrary.wiley.com/store/10.1002/ejic.200300725/asset/1427_ftp.pdf?v=1&t=h0dv48fi&s=e820b065a290bb56d412dedda0b8baf731808a0b-
heal.journalNameEuropean Journal of Inorganic Chemistryen
heal.journalTypepeer reviewed-
heal.languageen-
heal.publicationDate2004-
heal.publisherWiley-VCH Verlagen
heal.recordProviderΠανεπιστήμιο Ιωαννίνων. Σχολή Θετικών Επιστημών. Τμήμα Χημείαςel
heal.typejournalArticle-
heal.type.elΆρθρο Περιοδικούel
heal.type.enJournal articleen

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