Vaquero A, Portugal J
Departamento de Biología Molecular y Celular, Centro de Investigación y Desarrollo, CSIC, J. Girona-Salgado, Barcelona, Spain.
FEBS Lett. 1997 Dec 29;420(2-3):156-60. doi: 10.1016/s0014-5793(97)01509-3.
Three minor-groove binding ligands have been used to study the characteristics of two d(GA x CT)n DNAs embedded in longer DNA fragments. The binding of mithramycin, netropsin or Thia-Net to these sequences has been studied using DNAse I footprinting. None of these ligands appeared to bind to d(GA x CT)5 nor to d(GA x CT)22 extensively, although with mithramycin some protected bonds were detected at the very edge of these sequences. In general, these small ligands did not enhance the DNAse I cleavage patterns at the alternating d(GA x CT)n flanking sequences located near DNA regions where the drug was bound. The d(GA x CT)n sequences could act as a rigid block in which it is not easy to propagate structural changes, whereas other sequences flanking the binding sites showed cleavage enhancements.
三种小沟结合配体已被用于研究嵌入较长DNA片段中的两种d(GA x CT)n DNA的特性。使用DNA酶I足迹法研究了光神霉素、纺锤菌素或硫代纺锤菌素与这些序列的结合。这些配体似乎都没有广泛地结合到d(GA x CT)5或d(GA x CT)22上,尽管用光神霉素时在这些序列的最边缘检测到了一些受保护的键。一般来说,这些小配体并没有增强位于药物结合的DNA区域附近的交替d(GA x CT)n侧翼序列处的DNA酶I切割模式。d(GA x CT)n序列可以作为一个刚性模块,在其中不容易传播结构变化,而结合位点侧翼的其他序列则显示出切割增强。