کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1356617 | 981138 | 2008 | 7 صفحه PDF | دانلود رایگان |
The DNA binding efficacy and preferred mode of binding of a series of rhodamine-related chalcogenoxanthylium dyes was investigated by isothermal titration calorimetry (ITC) using ctDNA, [poly(dCdG)]2 and [poly(dAdT)]2, and by a topoisomerase I DNA unwinding (Topo I) assay. The dyes of this study showed tight binding to ctDNA with binding constants, Kb, on the order of 106–107 M−1. The ITC and Topo I assay studies suggested that the 9-substituent has a strong impact on binding modes ranging from an apparent preference for intercalation with a 9-2-thienyl substituent (similar binding to [poly(dCdG)]2 and [poly(dAdT)]2, re-supercoiling of DNA in the Topo I assay at <10−5 M dye), to mixed binding modes with 9-phenyl derivatives (2- to 3-fold preference for binding to [poly(dAdT)]2, re-supercoiling of DNA in the Topo I assay at ∼2 × 10−5 M dye), to minor groove binding in a 9-(2-thienyl-5-diethylcarboxamide) derivative (strong preference for binding to [poly(dAdT)]2, did not show complete re-supercoiling in the Topo I assay). No binding to ctDNA was observed in one derivative with a 9-(3-thienyl-2-diethylcarboxamide) substituent, which cannot be co-planar with the xanthylium core. In series of dyes where the chalcogen atom was varied, the selenoxanthylium derivatives had 2- to 3-fold higher values of Kb than the corresponding xanthylium, thioxanthylium, or telluroxanthylium derivatives, which all showed comparable values of Kb. The chalcogen atom appeared to have little influence on binding mode.
The binding of a series of rhodamine-related chalcogenoxanthylium dyes to DNA was measured using isothermal titration calorimetry and a topoisomerase I DNA unwinding assay.Figure optionsDownload as PowerPoint slide
Journal: Bioorganic & Medicinal Chemistry - Volume 16, Issue 24, 15 December 2008, Pages 10221–10227