Fussner-Dupas Eden, Li Ren, Strauss Mike
Department of Biochemistry and Molecular Biology, University of British Columbia, Vancouver, BC, Canada.
Cell Biology Program, Hospital for Sick Children, Toronto, ON, Canada.
Methods Mol Biol. 2025;2919:109-131. doi: 10.1007/978-1-0716-4486-7_7.
Generating three-dimensional element-specific images of chromatin, its surrounding protein, and RNA bodies is not routinely practiced in cell or structural biology, but it is an exceptional and powerful tool for understanding chromatin structure in situ. This electron microscopic technique may be a fruitful avenue for those interested in understanding local chromatin structure, the structure-functional relationship of histone modifications on gene expression, or phase separation and RNA regulation of the genome. Here, we describe an approach for performing correlative light and electron spectroscopic imaging tomography, which yields stunning high-resolution structures of chromatin in situ using elemental mapping. Traditional electron spectroscopic imaging (ESI), as all conventional transmission electron microscopy (TEM) image acquisition methods, is restricted to a single image plane, and consequently, information about the z-dimension is collapsed in the image. To overcome this projection limitation, electron tomography approaches are combined with energy-loss imaging; by acquiring and computationally combining a tilt series of image sets, the overlapping fibers of chromatin regions that appear indistinct in 2D are resolved to reveal their 3D architecture. Further combining this approach with correlative light images of the same physical section, structures which are associated with specific proteins of interest can be located and analyzed. Herein, we describe a detailed method for sample preparation, image acquisition, and data analysis and have attached in the Notes the scripts built in-house for ease of use.
生成染色质、其周围蛋白质和RNA体的三维元素特异性图像在细胞生物学或结构生物学中并非常规操作,但它是原位理解染色质结构的一种卓越且强大的工具。对于那些有兴趣了解局部染色质结构、组蛋白修饰对基因表达的结构-功能关系或基因组的相分离和RNA调控的人来说,这种电子显微镜技术可能是一条富有成果的途径。在这里,我们描述了一种进行相关光和电子光谱成像断层扫描的方法,该方法使用元素映射原位生成令人惊叹的染色质高分辨率结构。与所有传统透射电子显微镜(TEM)图像采集方法一样,传统电子光谱成像(ESI)仅限于单个图像平面,因此,关于z维度的信息在图像中被压缩。为了克服这种投影限制,电子断层扫描方法与能量损失成像相结合;通过获取并计算组合一系列倾斜的图像集,二维中看起来不清晰的染色质区域的重叠纤维得以解析,以揭示其三维结构。将这种方法与同一物理切片的相关光图像进一步结合,可以定位和分析与感兴趣的特定蛋白质相关的结构。在此,我们描述了一种详细的样品制备、图像采集和数据分析方法,并在注释中附上了内部编写的便于使用的脚本。