Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1988116 | International Journal of Biological Macromolecules | 2006 | 5 Pages |
Abstract
Novel acridine derivatives, wherein the steric factor has been varied systematically through substitution at the 9 position of the acridine ring, were evaluated as convenient fluorescent probes for nucleic acid detection. The binding affinities of N-(9-acridinylthiocarbamoyl)amino acids (ATA) with plasmid DNA (pUC 19) were investigated using UV–vis spectrophotometry, fluorometric titration and quantum chemical calculations (AM1). From spectrofluorometric analysis, the binding constants for the DNA-ATA complexes were determined. To elucidate its DNA intercalation, the most preferable tautomeric structure of ATA was established by means of AM1 calculations.
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Authors
D. Sabolová, M. Kožurková, P. Kristian, I. Danihel, D. Podhradský, J. Imrich,