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放线菌素D和阿霉素与超螺旋DNA、单链DNA及多核苷酸的结合。

The binding of actinomycin D and Adriamycin to supercoiled DNA, single-stranded DNA and polynucleotides.

作者信息

Simpkins H, Pearlman L F

出版信息

Biochim Biophys Acta. 1984 Dec 14;783(3):293-300. doi: 10.1016/0167-4781(84)90040-x.

Abstract

The effect of actinomycin D and adriamycin on synthetic polynucleotides, single-stranded viral DNA and supercoiled DNA has been studied employing the fluorescent probe, terbium. Marked displacement of the probe was observed when any deoxyribose-containing polynucleotide was pretreated with either drug. With supercoiled DNA, an unwinding of the supercoil was observed at very low drug concentrations (at approx. 1:500 molar ratio of drug:DNA) prior to the displacement of the terbium. This unwinding was visualized by agarose gel electrophoresis at molar ratios of approx. 1:200. The effect was more apparent and occurred at lower drug: DNA ratios with actinomycin D than with adriamycin. Unlike cis-dichlorodiammine platinum(II), actinomycin D did not protect pBR322 DNA from cleavage at its BamHI site. The hydrolysis of phi chi 174 DNA by a series of G-C-specific restriction nucleases (including HhaI, HpaII and HaeIII) was also not affected by prior treatment of the DNA with actinomycin D.

摘要

利用荧光探针铽研究了放线菌素D和阿霉素对合成多核苷酸、单链病毒DNA和超螺旋DNA的影响。当用这两种药物中的任何一种预处理任何含脱氧核糖的多核苷酸时,均观察到探针的明显位移。对于超螺旋DNA,在铽发生位移之前,在非常低的药物浓度下(药物与DNA的摩尔比约为1:500)观察到超螺旋解旋。通过琼脂糖凝胶电泳在约1:200的摩尔比下可观察到这种解旋。与阿霉素相比,放线菌素D的这种作用更明显,且在更低的药物与DNA比例下就会出现。与顺二氯二氨合铂(II)不同,放线菌素D不能保护pBR322 DNA在其BamHI位点处不被切割。用一系列G-C特异性限制性核酸酶(包括HhaI、HpaII和HaeIII)对φX174 DNA进行水解,也不受放线菌素D预先处理DNA的影响。

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