Werner James H, Cai Hong, Keller Richard A, Goodwin Peter M
Los Alamos National Laboratory, Bioscience Division, Los Alamos, New Mexico, USA.
Biophys J. 2005 Feb;88(2):1403-12. doi: 10.1529/biophysj.104.044255. Epub 2004 Nov 12.
We report heterogeneity in the time necessary for Exonuclease I to hydrolyze identical DNA fragments. A real-time fluorescence method measured the time required by molecules of Exonuclease I to hydrolyze single-stranded DNA that was synthesized to have two fluorescently labeled nucleotides. One fluorescently labeled nucleotide was located near the 3' end of the DNA and the other near the 5' end. Heterogeneity in the hydrolysis rate of the exonuclease population was inferred from the distribution of times necessary to cleave these DNA fragments. In particular, we found simple first-order kinetics, using a single hydrolysis rate, did not result in a good fit to the data. Better fits to the data were obtained if one assumed a distribution of hydrolysis rates for the exonuclease population. Under our experimental conditions, this broad distribution of rates was centered near 100 nt/s.
我们报告了核酸外切酶I水解相同DNA片段所需时间的异质性。一种实时荧光方法测量了核酸外切酶I分子水解合成的具有两个荧光标记核苷酸的单链DNA所需的时间。一个荧光标记核苷酸位于DNA的3'端附近,另一个位于5'端附近。从切割这些DNA片段所需时间的分布推断出核酸外切酶群体水解速率的异质性。特别是,我们发现使用单一水解速率的简单一级动力学并不能很好地拟合数据。如果假设核酸外切酶群体的水解速率分布,则能更好地拟合数据。在我们的实验条件下,这种广泛的速率分布集中在100 nt/s附近。