Azadnia A, Campbell R, Sharma M
Department of Biophysics, Roswell Park Cancer Institute, Buffalo, New York 14263.
Anal Biochem. 1994 May 1;218(2):444-8. doi: 10.1006/abio.1994.1204.
The 5'-phosphate groups of the normal nucleotides of DNA (10 nmol) were labeled with two different fluorescent reagents, namely, dansyl chloride and fluorescein-isothiocyanate, via phosphoramidate derivatives of ethylene and hexamethylenediamines. Using a conventional detector, HPLC analysis showed a linear relationship of fluorescence signal as an integrated peak area and the amounts of nucleotide injected from 2 pmol to 200 fmol (r = 0.996, n = 3) for dansyl-labeled dAmp and from 2 pmol to 90 fmol (r = 0.997) for fluorescein-labeled dAmp, respectively. Although fluorescein-labeled nucleotides are more sensitive than dansylated nucleotides (detection limit < 2 times, S/N = 3), the excess labeling reagent from the fluorescein labeling reaction interferes with HPLC resolution of the labeled nucleotides. The phosphoramidate derivatives of the nucleotides require purification prior to labeling with fluorescein isothiocyanate. As a result, the overall assay procedure becomes complicated. The potential of dansylated nucleotides to assay DNA modifications has been demonstrated by HPLC resolution of the labeled nucleotides of both normal and modified bases without further manipulation of the reaction intermediates.
DNA的正常核苷酸(10 nmol)的5'-磷酸基团通过乙烯和六亚甲基二胺的氨基磷酸酯衍生物,用两种不同的荧光试剂即丹磺酰氯和异硫氰酸荧光素进行标记。使用传统检测器,HPLC分析表明,对于丹磺酰基标记的dAmp,荧光信号作为积分峰面积与注入的核苷酸量在2 pmol至200 fmol之间呈线性关系(r = 0.996,n = 3),对于异硫氰酸荧光素标记的dAmp,在2 pmol至90 fmol之间呈线性关系(r = 0.997)。尽管异硫氰酸荧光素标记的核苷酸比丹磺酰化的核苷酸更灵敏(检测限<2倍,S/N = 3),但异硫氰酸荧光素标记反应中过量的标记试剂会干扰标记核苷酸的HPLC分离。核苷酸的氨基磷酸酯衍生物在用异硫氰酸荧光素标记之前需要进行纯化。结果,整个测定过程变得复杂。通过对正常碱基和修饰碱基的标记核苷酸进行HPLC分离,在无需对反应中间体进行进一步操作的情况下,已证明了丹磺酰化核苷酸用于检测DNA修饰的潜力。