BioNano Laboratory, Biological Engineering, University of Guelph, Guelph, Ontario, N1G 2 W1, Canada.
Nanoscale Res Lett. 2013 Nov 6;8(1):463. doi: 10.1186/1556-276X-8-463.
Here we present a high-resolution chromosomal spectral map derived from synchrotron-based soft X-ray spectromicroscopy applied to quinoa species. The label-free characterization of quinoa metaphase chromosomes shows that it consists of organized substructures of DNA-protein complex. The analysis of spectra of chromosomes using the scanning transmission X-ray microscope (STXM) and its superposition of the pattern with the atomic force microscopy (AFM) and scanning electron microscopy (SEM) images proves that it is possible to precisely locate the gene loci and the DNA packaging inside the chromosomes. STXM has been successfully used to distinguish and quantify the DNA and protein components inside the quinoa chromosomes by visualizing the interphase at up to 30-nm spatial resolution. Our study represents the successful attempt of non-intrusive interrogation and integrating imaging techniques of chromosomes using synchrotron STXM and AFM techniques. The methodology developed for 3-D imaging of chromosomes with chemical specificity and temporal resolution will allow the nanoscale imaging tools to emerge from scientific research and development into broad practical applications such as gene loci tools and biomarker libraries.
在这里,我们呈现了一张源自同步辐射软 X 射线光谱显微镜应用于藜麦物种的高分辨率染色体能谱图。藜麦中期染色体的无标记特征表明,它由 DNA-蛋白质复合物的有组织亚结构组成。使用扫描透射 X 射线显微镜(STXM)对染色体光谱的分析及其与原子力显微镜(AFM)和扫描电子显微镜(SEM)图像的叠加证明,精确定位基因座和染色体内部的 DNA 包装是可能的。STXM 已成功用于通过可视化高达 30nm 空间分辨率的相间,区分和量化藜麦染色体内部的 DNA 和蛋白质成分。我们的研究代表了使用同步辐射 STXM 和 AFM 技术对染色体进行非侵入性询问和整合成像技术的成功尝试。开发的具有化学特异性和时间分辨率的染色体三维成像方法将允许纳米级成像工具从科学研究和开发中发展到广泛的实际应用,例如基因座工具和生物标志物库。