Liu M S, Zang J, Evangelista R A, Rampal S, Chen F T
Advanced Technology Center, D-20-A, Beckman Instruments, Fullerton, CA 92634, USA.
Biotechniques. 1995 Feb;18(2):316-7, 320, 322-3.
We have developed a rapid and sensitive method to analyze double-stranded DNA by capillary electrophoresis equipped with a laser-induced fluorescence detector. Using ethidium bromide as an intercalator in polyacrylamide gel-filled capillaries along with a green He/Ne laser source (excitation: 543 nm; emission: 600 nm), we found the detection sensitivity for a single DNA-ethidium bromide complex was in the picogram level with a resolution of one base pair separation between two DNA fragments. In the case of the separation of a phi X174 DNA-HaeIII digest, sizes from 72 to 1353 bp were well resolved within 12 min. For the analysis of PCR-amplified DNA, low levels of amplified DNA fragments could be detected that could not be visualized in agarose gel after standard ethidium bromide staining. Considering the high resolving power and sensitivity, we believe that this method can be a useful tool for the analysis of double-stranded DNA especially for PCR-amplified DNA fragments.
我们开发了一种快速灵敏的方法,通过配备激光诱导荧光检测器的毛细管电泳来分析双链DNA。在填充聚丙烯酰胺凝胶的毛细管中使用溴化乙锭作为嵌入剂,并结合绿色氦氖激光源(激发波长:543nm;发射波长:600nm),我们发现单个DNA-溴化乙锭复合物的检测灵敏度处于皮克水平,两个DNA片段之间的分辨率可达一个碱基对。在分离φX174 DNA-HaeIII酶切片段的情况下,72至1353bp大小的片段在12分钟内得到了很好的分离。对于PCR扩增DNA的分析,能够检测到低水平的扩增DNA片段,这些片段在标准溴化乙锭染色后在琼脂糖凝胶中无法可视化。考虑到高分辨率和灵敏度,我们认为该方法可成为分析双链DNA尤其是PCR扩增DNA片段的有用工具。