Żurek-Biesiada Dominika, Szczurek Aleksander T, Prakash Kirti, Mohana Giriram K, Lee Hyun-Keun, Roignant Jean-Yves, Birk Udo J, Dobrucki Jurek W, Cremer Christoph
Laboratory of Cell Biophysics, Faculty of Biochemistry, Biophysics and Biotechnology, Jagiellonian University, Gronostajowa 7, 30-387 Kraków, Poland.
Institute of Molecular Biology (IMB), Ackermannweg 4, 55128 Mainz, Germany.
Exp Cell Res. 2016 May 1;343(2):97-106. doi: 10.1016/j.yexcr.2015.08.020. Epub 2015 Sep 1.
Higher order chromatin structure is not only required to compact and spatially arrange long chromatids within a nucleus, but have also important functional roles, including control of gene expression and DNA processing. However, studies of chromatin nanostructures cannot be performed using conventional widefield and confocal microscopy because of the limited optical resolution. Various methods of superresolution microscopy have been described to overcome this difficulty, like structured illumination and single molecule localization microscopy. We report here that the standard DNA dye Vybrant(®) DyeCycle™ Violet can be used to provide single molecule localization microscopy (SMLM) images of DNA in nuclei of fixed mammalian cells. This SMLM method enabled optical isolation and localization of large numbers of DNA-bound molecules, usually in excess of 10(6) signals in one cell nucleus. The technique yielded high-quality images of nuclear DNA density, revealing subdiffraction chromatin structures of the size in the order of 100nm; the interchromatin compartment was visualized at unprecedented optical resolution. The approach offers several advantages over previously described high resolution DNA imaging methods, including high specificity, an ability to record images using a single wavelength excitation, and a higher density of single molecule signals than reported in previous SMLM studies. The method is compatible with DNA/multicolor SMLM imaging which employs simple staining methods suited also for conventional optical microscopy.
高阶染色质结构不仅对于在细胞核内压缩和空间排列长染色单体是必需的,而且还具有重要的功能作用,包括基因表达的控制和DNA加工。然而,由于光学分辨率有限,无法使用传统的宽场和共聚焦显微镜对染色质纳米结构进行研究。已经描述了各种超分辨率显微镜方法来克服这一困难,如结构光照和单分子定位显微镜。我们在此报告,标准DNA染料Vybrant(®) DyeCycle™ Violet可用于提供固定哺乳动物细胞核中DNA的单分子定位显微镜(SMLM)图像。这种SMLM方法能够对大量与DNA结合的分子进行光学分离和定位,通常在一个细胞核中超过10^6个信号。该技术产生了高质量的核DNA密度图像,揭示了尺寸约为100nm的亚衍射染色质结构;染色质间区以前所未有的光学分辨率可视化。与先前描述的高分辨率DNA成像方法相比,该方法具有几个优点, 包括高特异性、使用单波长激发记录图像的能力以及比先前SMLM研究中报道的更高密度的单分子信号。该方法与DNA/多色SMLM成像兼容,后者采用也适用于传统光学显微镜的简单染色方法。