Department of Chemistry, University of Pittsburgh, 219 Parkman Avenue, Pittsburgh, PA, 15260, USA.
Division of Biological, Chemical, and Environmental Sciences, Westminster College, 319 S Market St., New Wilmington, PA, 16172, USA.
Angew Chem Int Ed Engl. 2017 Feb 13;56(8):2115-2117. doi: 10.1002/anie.201611197. Epub 2017 Jan 16.
A site-specific Cu binding motif within a DNA duplex for distance measurements by ESR spectroscopy is reported. This motif utilizes a commercially available 2,2'-dipicolylamine (DPA) phosphormadite easily incorporated into any DNA oligonucleotide during initial DNA synthesis. The method only requires the simple post-synthetic addition of Cu without the need for further chemical modification. Notably, the label is positioned within the DNA duplex, as opposed to outside the helical perimeter, for an accurate measurement of duplex distance. A distance of 2.7 nm was measured on a doubly Cu -labeled DNA sequence, which is in exact agreement with the expected distance from both DNA modeling and molecular dynamic simulations. This result suggests that with this labeling strategy the ESR measured distance directly reports on backbone DNA distance, without the need for further modeling. Furthermore, the labeling strategy is structure- and nucleotide-independent.
本文报道了一种在 DNA 双链中用于通过 ESR 光谱法进行距离测量的特定 Cu 结合基序。该基序利用一种市售的 2,2'-二吡啶基胺 (DPA) 膦酸甲酯,在初始 DNA 合成过程中很容易掺入任何 DNA 寡核苷酸中。该方法只需要在合成后简单地添加 Cu,而无需进一步的化学修饰。值得注意的是,该标签位于 DNA 双链内,而不是在螺旋轮廓之外,可实现对双链距离的精确测量。在双 Cu 标记的 DNA 序列上测量到 2.7nm 的距离,这与从 DNA 建模和分子动力学模拟得出的预期距离完全一致。这一结果表明,通过这种标记策略,ESR 测量的距离直接反映了 DNA 骨架的距离,而无需进一步建模。此外,该标记策略与结构和核苷酸无关。