Vladescu Ioana D, McCauley Micah J, Nuñez Megan E, Rouzina Ioulia, Williams Mark C
Department of Physics, Northeastern University, Boston, Massachusetts 02115, USA.
Nat Methods. 2007 Jun;4(6):517-22. doi: 10.1038/nmeth1044. Epub 2007 Apr 29.
We used single DNA molecule stretching to investigate DNA intercalation by ethidium and three ruthenium complexes. By measuring ligand-induced DNA elongation at different ligand concentrations, we determined the binding constant and site size as a function of force. Both quantities depend strongly on force and, in the limit of zero force, converge to the known bulk solution values, when available. This approach allowed us to distinguish the intercalative mode of ligand binding from other binding modes and allowed characterization of intercalation with binding constants ranging over almost six orders of magnitude, including ligands that do not intercalate under experimentally accessible solution conditions. As ligand concentration increased, the DNA stretching curves saturated at the maximum amount of ligand intercalation. The results showed that the applied force partially relieves normal intercalation constraints. We also characterized the flexibility of intercalator-saturated dsDNA for the first time.
我们使用单分子DNA拉伸技术研究了溴化乙锭和三种钌配合物对DNA的嵌入作用。通过测量不同配体浓度下配体诱导的DNA伸长,我们确定了结合常数和位点大小与力的函数关系。这两个量都强烈依赖于力,并且在零力的极限情况下,当有可用数据时,会收敛到已知的本体溶液值。这种方法使我们能够区分配体结合的嵌入模式与其他结合模式,并能够表征结合常数范围跨越近六个数量级的嵌入作用,包括在实验可及的溶液条件下不发生嵌入的配体。随着配体浓度的增加,DNA拉伸曲线在最大配体嵌入量时达到饱和。结果表明,施加的力部分缓解了正常的嵌入限制。我们还首次表征了嵌入剂饱和的双链DNA的柔韧性。