Ford K, Fox K R, Neidle S, Waring M J
Nucleic Acids Res. 1987 Mar 11;15(5):2221-34. doi: 10.1093/nar/15.5.2221.
The DNA sequence preferences of the compound meso-tetra-(4-N-methyl(pyridyl) porphyrin and its nickel complex have been investigated by means of footprinting experiments on several DNA fragments, using DNAase I and micrococcal nuclease as footprinting agents. A complex pattern of both AT and GC-protected sites was found. Ligand-induced long-range conformational changes were inferred in several instances to be related to the observed large-scale blockages of enzymatic cutting.
通过使用脱氧核糖核酸酶I和微球菌核酸酶作为足迹试剂,对几个DNA片段进行足迹实验,研究了化合物中-四-(4-N-甲基(吡啶基)卟啉及其镍配合物的DNA序列偏好。发现了由AT和GC保护位点组成的复杂模式。在几种情况下,推断配体诱导的长程构象变化与观察到的酶切大规模阻断有关。