Berge Torunn, Jenkins Nigel S, Hopkirk Richard B, Waring Michael J, Edwardson J Michael, Henderson Robert M
Department of Pharmacology, University of Cambridge, Tennis Court Road, Cambridge CB2 1PD, UK.
Nucleic Acids Res. 2002 Jul 1;30(13):2980-6. doi: 10.1093/nar/gkf409.
Atomic force microscopy (AFM) has been used to examine perturbations in the tertiary structure of DNA induced by the binding of ditercalinium, a DNA bis-intercalator with strong anti-tumour properties. We report AFM images of plasmid DNA of both circular and linearised forms showing a difference in the formation of supercoils and plectonemic coils caused at least in part by alterations in the superhelical stress upon bis-intercalation. A further investigation of the effects of drug binding performed with 292 bp mixed-sequence DNA fragments, and using increment in contour length as a reliable measure of intercalation, revealed saturation occurring at a point where sufficient drug was present to interact with every other available binding site. Moment analysis based on the distribution of angles between segments along single DNA molecules showed that at this level of bis-intercalation, the apparent persistence length of the molecules was 91.7 +/- 5.7 nm, approximately twice as long as that of naked DNA. We conclude that images of single molecules generated using AFM provide a valuable supplement to solution-based techniques for evaluation of physical properties of biological macromolecules.
原子力显微镜(AFM)已被用于检测由双特卡林ium(一种具有强大抗肿瘤特性的DNA双嵌入剂)结合所诱导的DNA三级结构扰动。我们报告了环状和线性化形式的质粒DNA的AFM图像,这些图像显示了超螺旋和麻花状螺旋的形成差异,这至少部分是由双嵌入时超螺旋应力的改变引起的。使用292 bp混合序列DNA片段对药物结合的影响进行的进一步研究,并将轮廓长度的增加作为嵌入的可靠指标,结果表明,当存在足够的药物与每隔一个可用结合位点相互作用时,会出现饱和现象。基于单个DNA分子上各片段之间角度分布的矩分析表明,在这种双嵌入水平下,分子的表观持久长度为91.7 +/- 5.7 nm,约为裸DNA的两倍。我们得出结论,使用AFM生成的单分子图像为基于溶液的技术评估生物大分子的物理性质提供了有价值的补充。