Macgregor R B
Department of Medicinal Chemistry and Pharmacognosy, University of Illinois, Chicago 60680.
Anal Biochem. 1992 Aug 1;204(2):324-7. doi: 10.1016/0003-2697(92)90246-4.
Hydroxyl radicals yield footprints of DNA-ligand interactions that are uniform in intensity and display single base pair resolution. It is shown here that brief illumination of dilute aqueous solutions of hydrogen peroxide with a standard uv transilluminator can be used to generate hydroxyl radicals for footprinting studies. Photogenerated hydroxyl radicals are used to footprint netropsin, a drug that interacts with the minor groove of DNA. The method presented eliminates two of the reagents used in conventional Fenton-reaction-based hydroxyl radical footprinting. It has the further advantage that the extent of cleavage of the DNA can be precisely regulated by controlling the illumination time. Because light is used to drive the reaction, photogenerated hydroxyl radicals can be used to footprint DNA-ligand interactions under experimental conditions of temperature and pressure inaccessible to Fenton-reaction chemistry.
羟基自由基产生的DNA-配体相互作用足迹在强度上是均匀的,并显示出单碱基对分辨率。本文表明,用标准紫外透射仪短暂照射过氧化氢稀水溶液可用于产生羟基自由基以进行足迹研究。光生羟基自由基用于对与DNA小沟相互作用的药物纺锤菌素进行足迹分析。所提出的方法省去了传统的基于芬顿反应的羟基自由基足迹分析中使用的两种试剂。它还有一个进一步的优点,即可以通过控制光照时间精确调节DNA的切割程度。由于使用光来驱动反应,光生羟基自由基可用于在芬顿反应化学无法达到的温度和压力实验条件下对DNA-配体相互作用进行足迹分析。