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Interaction of 7-aminoactinomycin D with single- and double-stranded DNA oligonucleotides

机译:7-氨基酰胺霉素D与单链和双链DNA寡核苷酸的相互作用

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7-Aminoactinomycin D is a potent inhibitor of RNA polymerase and it has been demonstrated to bind to a single stranded DNA. Wadkins and Jovin showed that there is a 20 to 40 fold enhancement in the fluorescence of 7-aminoactinomycin D upon binding to certain single stranded DNA sequences. We report studies of the thermodynamics of the binding of the parent drug, actinomycin D, to single and double stranded DNA. A five-fold range of association constants is found for the different binding sequences that we have investigated. We will correlate these thermodynamic studies with measurements of the fluorescence enhancement, lifetime, and rotational correlation time of the drug bound to the various single and double stranded oligonucleotides.
机译:7-氨基酰胺霉素D是RNA聚合酶的有效抑制剂,并且已经证明了与单链DNA结合。幼女和Jovin表明,在与某些单链DNA序列结合后,7-氨基酰亚胺霉素D的荧光增加了20至40倍。我们报告了对母体药物,放线霉素D的结合的热力学的研究,对单链和双链DNA。发现了五个关联常数范围用于我们研究的不同结合序列。我们将通过测量与各种单链和双链寡核苷酸结合的药物的荧光增强,寿命和旋转相关时间来关联这些热力学研究。

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