Tullius T D, Dombroski B A
Proc Natl Acad Sci U S A. 1986 Aug;83(15):5469-73. doi: 10.1073/pnas.83.15.5469.
A method has been developed for making "footprints" of proteins bound to DNA. The hydroxyl radical, generated by reduction of hydrogen peroxide by iron(II), is the reagent used to cut the DNA. Hydroxyl radical breaks the backbone of DNA with almost no sequence dependence, so all backbone positions may be monitored for contact with protein. In addition to defining the DNA sequence in contact with the protein, hydroxyl radical footprints embody structural information about the DNA-protein complex. For example, hydroxyl radical footprints of the bacteriophage lambda repressor and Cro protein show directly that these proteins are bound to only one side of the DNA helix. Additional contacts of lambda repressor and Cro protein with DNA, not observed by other chemical footprinting methods, are revealed by hydroxyl radical footprinting.
一种用于制作与DNA结合的蛋白质“足迹”的方法已经开发出来。由铁(II)还原过氧化氢产生的羟基自由基是用于切割DNA的试剂。羟基自由基几乎不依赖序列地断裂DNA主链,因此可以监测所有主链位置与蛋白质的接触情况。除了确定与蛋白质接触的DNA序列外,羟基自由基足迹还体现了关于DNA-蛋白质复合物的结构信息。例如,噬菌体λ阻遏蛋白和Cro蛋白的羟基自由基足迹直接表明这些蛋白质仅与DNA螺旋的一侧结合。羟基自由基足迹揭示了λ阻遏蛋白和Cro蛋白与DNA的其他接触,而这些接触是其他化学足迹方法所未观察到的。