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Caffeine clusters as transmitters of actinomycin antibiotics to DNA in solution

机译:咖啡因簇集放线菌素抗生素向溶液中的DNA传递

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摘要

Using the screening model of hypochromism, we showed that caffeine forms regular clusters consisting of 8–12 molecules. Addition of 7-aminoactinomycin D (7AAMD, a fluorescent analogue of actinomycin D) to the clusters leads to its sorption on the cluster surface. Photoexcitation of 7AAMD leads to its desorption from the surface into the aqueous phase and emission of a quantum. Fluorescence of 7AAMD in the presence of caffeine clusters is quenched by dinitrophenol more weakly than without clusters (the quenching constants are ~ 85 and ~280 M?1, respectively) due to decreased steric availability of the antibiotic to the quencher. Addition of 7AAMD-caffeine complexes to DNA leads to a long-wavelength shift in the excitation spectrum and an increase in the fluorescence intensity along with a shift of the fluorescence spectrum to the short-wavelength area. This fact reflects redistribution of the antibiotic from the caffeine surface to the hydrophobic areas inside DNA.
机译:使用低色度的筛选模型,我们表明咖啡因形成由8-12个分子组成的规则簇。向簇中添加7-氨基放线菌素D(7AAMD,放线菌素D的荧光类似物)导致其在簇表面上的吸附。 7AAMD的光激发导致其从表面解吸到水相中并发射出量子。在咖啡因簇存在下,7AAMD的荧光被二硝基苯酚的猝灭作用比没有簇时更弱(猝灭常数分别为〜85和280 M?1),这是由于抗生素对猝灭剂的空间利用率降低。将7AAMD-咖啡因复合物添加到DNA中会导致激发光谱发生长波移,荧光强度增加,同时荧光光谱移至短波区域。这一事实反映了抗生素从咖啡因表面到DNA内部疏水区域的重新分布。

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