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An overview of DNA and RNA bindings to antioxidant flavonoids

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dc.contributor.advisor Tajmir-Riahi, Heidar Ali en
dc.contributor.author Kanakis, Charalabos D. en
dc.contributor.author Tarantilis, Petros A. en
dc.contributor.author Polissiou, Moschos en
dc.contributor.author Diamantoglou, Stavroula en
dc.contributor.author Διαμάντογλου, Σταυρούλα el
dc.contributor.author Ταραντίλης, Πέτρος Α. el
dc.contributor.author Πολυσίου, Μόσχος el
dc.contributor.author Κανάκης, Χαράλαμπος Δ. el
dc.date.accessioned 2014-06-06T06:47:59Z
dc.date.available 2014-06-06T06:47:59Z
dc.date.issued 2007-09 en
dc.identifier.issn 10859195 en
dc.identifier.uri http://dx.doi.org/10.1007/s12013-007-0037-2 en
dc.identifier.uri http://62.217.125.90/xmlui/handle/123456789/3904
dc.title An overview of DNA and RNA bindings to antioxidant flavonoids en
heal.keyword Antioxidant en
heal.keyword Binding constant en
heal.keyword Binding sites en
heal.keyword DNA en
heal.keyword Flavonoids en
heal.keyword FT-IR en
heal.keyword tRNA en
heal.keyword UV-Visible en
heal.keyword Spectroscopy en
heal.keyword Anthocyanin en
heal.keyword Delphinidin en
heal.keyword Kaempferols en
heal.keyword RNA en
heal.keyword Kinetics en
heal.keyword Quercetin en
heal.keyword Transfer RNA en
heal.identifier.primary 10.1007/s12013-007-0037-2 en
heal.recordProvider University of Quebec at Trois-Rivieres/Department of Chemistry-Biology en
heal.recordProvider Γεωπονικό Πανεπιστήμιο Αθηνών/Γενικό Τμήμα el
heal.publicationDate 2007-09 en
heal.bibliographicCitation Tajmir-Riahi, Heidar Ali. An overview of DNA and RNA bindings to antioxidant flavonoids. Cell Biochemistry & Biophysics, vol. 49 (1), pp. 29-36, Humana Press 2007 en
heal.abstract In this report we are examining how the antioxidant flavonoids can prevent DNA damage and what mechanism of action is involved in the process. Flavonoids are strong antioxidants that prevent DNA damage. The anticancer and antiviral activities of these natural products are implicated in their mechanism of actions. We study the interactions of quercetin (que), kaempferol (kae), and delphinidin (del) with DNA and transfer RNA in aqueous solution at physiological conditions, using constant DNA or RNA concentration 6.25 mmol (phosphate) and various pigment/polynucleotide(phosphate) ratios of 1/65 to 1 (DNA) and 1/48 to 1/8 (tRNA). The structural analysis showed quercetin, kaempferol, and delphinidin intercalate DNA and RNA duplexes with minor external binding to the major or minor groove and the backbone phosphate group with overall binding constants for DNA adducts Kque = 7.25 (±0.65) × 104 M-1, Kkae = 3.60 (±0.33) × 104 M-1, and Kdel = 1.66 (±0.25) × 104 M-1 and for tRNA adducts Kque = 4.80 (±0.50) × 104 M-1, Kkae = 4.65 (±0.45) × 104 M-1, and Kdel = 9.47 (±0.70) × 104 M1. The stability of adduct formation is in the order of del>que>kae for tRNA and que>kae>del for DNA. Low flavonoid concentration induces helical stabilization, whereas high pigment content causes helix opening. A partial B to A-DNA transition occurs at high drug concentration, while tRNA remains in A-family structure. The antioxidant activity of flavonoids changes in order delphinidin>quercetin>kaempferol. The results show intercalated flavonoids can make them strong antioxidants to protect DNA from harmful free radical reactions. © Humana Press Inc. 2007. en
heal.publisher Humana Press en
heal.journalName Cell Biochemistry and Biophysics en
dc.identifier.doi 10.1007/s12013-007-0037-2 en


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