Maschmann April, Masters Cody, Davison Melissa, Lallman Joshua, Thompson Drew, Kounovsky-Shafer Kristy L
Department of Chemistry, University of Nebraska - Kearney.
Department of Chemistry, University of Nebraska - Kearney;
J Vis Exp. 2018 Feb 2(132):57141. doi: 10.3791/57141.
Visualization of DNA for fluorescence microscopy utilizes a variety of dyes such as cyanine dyes. These dyes are utilized due to their high affinity and sensitivity for DNA. In order to determine if the DNA molecules are full length after the completion of the experiment, a method is required to determine if the stained molecules are full length by digesting DNA with restriction enzymes. However, stained DNA may inhibit the enzymes, so a method is needed to determine what enzymes one could use for fluorochrome stained DNA. In this method, DNA is stained with a cyanine dye overnight to allow the dye and DNA to equilibrate. Next, stained DNA is digested with a restriction enzyme, loaded into a gel and electrophoresed. The experimental DNA digest bands are compared to an in silico digest to determine the restriction enzyme activity. If there is the same number of bands as expected, then the reaction is complete. More bands than expected indicate partial digestion and less bands indicate incomplete digestion. The advantage of this method is its simplicity and it uses equipment that a scientist would need for a restriction enzyme assay and gel electrophoresis. A limitation of this method is that the enzymes available to most scientists are commercially available enzymes; however, any restriction enzymes could be used.
用于荧光显微镜观察的DNA可视化技术使用了多种染料,如菁染料。使用这些染料是因为它们对DNA具有高亲和力和敏感性。为了在实验完成后确定DNA分子是否全长,需要一种方法,即通过用限制酶消化DNA来确定染色后的分子是否全长。然而,染色的DNA可能会抑制酶的活性,因此需要一种方法来确定哪些酶可用于荧光染料染色的DNA。在该方法中,DNA用菁染料染色过夜,以使染料和DNA达到平衡。接下来,用限制酶消化染色的DNA,将其加载到凝胶中并进行电泳。将实验性DNA消化条带与计算机模拟消化结果进行比较,以确定限制酶的活性。如果条带数量与预期相同,则反应完成。条带数量多于预期表明部分消化,条带数量少于预期表明消化不完全。该方法的优点是简单,并且使用了科学家进行限制酶分析和凝胶电泳所需的设备。该方法的一个局限性是,大多数科学家可获得的酶是商业上可买到的酶;然而,任何限制酶都可以使用。