Dickman Mark J
Department of Chemical and Process Engineering, Biological and Environmental Systems, University of Sheffield, Sheffield S1 3JD, UK.
Anal Biochem. 2007 Jan 15;360(2):282-7. doi: 10.1016/j.ab.2006.09.034. Epub 2006 Oct 18.
Here we report a simple and effective procedure enabling the fluorescent detection of nucleic acids following the rapid, high-resolution separation using ion pair reverse phase chromatography. This approach uses postcolumn nucleic acid intercalation of fluorescent dyes with subsequent fluorescent detection, demonstrating more than a 1000-fold increase in sensitivity in the detection of nucleic acids when compared with traditional UV detection. Moreover, a wide range of intercalating dyes can be incorporated, including those known to disrupt the structure of the nucleic acids, thereby enabling the sensitive detection of DNA and RNA with no adverse effect on resolution of the nucleic acids during ion pair reverse phase chromatography. In addition, such approaches allow one to readily distinguish single-stranded DNA from double-stranded DNA following their separation using ion pair reverse phase high-performance liquid chromatography.
在此,我们报告了一种简单有效的方法,该方法能够在使用离子对反相色谱进行快速、高分辨率分离后对核酸进行荧光检测。这种方法利用荧光染料的柱后核酸嵌入及随后的荧光检测,与传统紫外检测相比,在核酸检测中灵敏度提高了1000倍以上。此外,可以加入多种嵌入染料,包括那些已知会破坏核酸结构的染料,从而能够灵敏地检测DNA和RNA,且对离子对反相色谱过程中核酸的分离分辨率没有不利影响。此外,这种方法可以让人在使用离子对反相高效液相色谱分离后轻松区分单链DNA和双链DNA。