Fletcher M C, Fox K R
Department of Physiology and Pharmacology, University of Southampton, UK.
Nucleic Acids Res. 1993 Mar 25;21(6):1339-44. doi: 10.1093/nar/21.6.1339.
We have investigated the kinetics of dissociation of actinomycin D from DNA by a variation of the footprinting technique. Complexes of actinomycin with a radiolabelled DNA fragment (tyrT) were dissociated by addition of a large excess of unlabelled calf thymus DNA and the mixture subjected to DNase I footprinting at subsequent intervals. The rates at which the footprints disappeared varied between the different binding sites. The dissociation was temperature dependent with average time constants of 30 s, 10 mins and 2 hours at temperatures of 37 degrees C, 20 degrees C and 4 degrees C respectively. The dissociation from a DNA fragment containing the synthetic insert T9GCA9 was significantly faster, with a half-life of about 1 min at 20 degrees C. In contrast, the dissociation of distamycin was too fast to measure (< 5 s) even at 4 degrees C.
我们通过足迹技术的一种变体研究了放线菌素D从DNA上解离的动力学。通过加入大量过量的未标记小牛胸腺DNA,使放线菌素与放射性标记的DNA片段(tyrT)形成的复合物解离,并在随后的不同时间间隔对混合物进行DNase I足迹分析。不同结合位点处足迹消失的速率各不相同。解离过程与温度有关,在37℃、20℃和4℃时的平均时间常数分别为30秒、10分钟和2小时。从含有合成插入片段T9GCA9的DNA片段上的解离明显更快,在20℃时半衰期约为1分钟。相比之下,即使在4℃时,偏端霉素的解离也太快而无法测量(<5秒)。