Mendel D, Dervan P B
Proc Natl Acad Sci U S A. 1987 Feb;84(4):910-4. doi: 10.1073/pnas.84.4.910.
Forms of the DNA double helix containing non-Watson-Crick base-pairing have been discovered recently based on x-ray diffraction analysis of quinoxaline antibiotic-oligonucleotide complexes. In an effort to find evidence for Hoogsteen base-pairing at quinoxaline-binding sites in solution, chemical "footprinting" (differential cleavage reactivity) of echinomycin bound to DNA restriction fragments was examined. We report that purines (A greater than G) in the first and/or fourth base-pair positions of occupied echinomycin-binding sites are hyperreactive to diethyl pyrocarbonate. The correspondence of the solid-state data and the sites of diethyl pyrocarbonate hyperreactivity suggests that diethyl pyrocarbonate may be a sensitive reagent for the detection of Hoogsteen base-pairing in solution. Moreover, a 12-base-pair segment of alternating A-T DNA, which is 6 base pairs away from the nearest strong echinomycin-binding site, is also hyperreactive to diethyl pyrocarbonate in the presence of echinomycin. This hyperreactive segment may be an altered form of right-handed DNA that is entirely Hoogsteen base-paired.
基于喹喔啉抗生素 - 寡核苷酸复合物的X射线衍射分析,最近发现了含有非沃森 - 克里克碱基配对的DNA双螺旋形式。为了寻找溶液中喹喔啉结合位点处霍格施泰因碱基配对的证据,研究了与DNA限制片段结合的棘霉素的化学“足迹”(差异切割反应性)。我们报告说,在被占据的棘霉素结合位点的第一和/或第四碱基对位置的嘌呤(A大于G)对焦碳酸二乙酯具有高反应性。固态数据与焦碳酸二乙酯高反应性位点的对应关系表明,焦碳酸二乙酯可能是检测溶液中霍格施泰因碱基配对的灵敏试剂。此外,在棘霉素存在下,与最近的强棘霉素结合位点相距6个碱基对的交替A - T DNA的12碱基对片段对焦碳酸二乙酯也具有高反应性。这个高反应性片段可能是完全由霍格施泰因碱基配对构成的右手DNA的一种改变形式。