Paul Scherrer Institute (PSI) , 5232 Villigen, Switzerland.
ACS Nano. 2016 May 24;10(5):4981-8. doi: 10.1021/acsnano.6b01328. Epub 2016 Apr 19.
Electron microscopy (EM) entered a new era with the emergence of direct electron detectors and new nanocrystal electron diffraction methods. However, sample preparation techniques have not progressed and still suffer from extensive blotting steps leading to a massive loss of sample. Here, we present a simple but versatile method for the almost lossless sample conditioning and preparation of nanoliter volumes of biological samples for EM, keeping the sample under close to physiological condition. A microcapillary is used to aspirate 3-5 nL of sample. The microcapillary tip is immersed into a reservoir of negative stain or trehalose, where the sample becomes conditioned by diffusive exchange of salt and heavy metal ions or sugar molecules, respectively, before it is deposited as a small spot onto an EM grid. We demonstrate the use of the method to prepare protein particles for imaging by transmission EM and nanocrystals for analysis by electron diffraction. Furthermore, the minute sample volume required for this method enables alternative strategies for biological experiments, such as the analysis of the content of a single cell by visual proteomics, fully exploiting the single molecule detection limit of EM.
电子显微镜(EM)随着直接电子探测器和新的纳米晶体电子衍射方法的出现进入了一个新时代。然而,样品制备技术并没有进步,仍然存在广泛的印迹步骤,导致大量的样品损失。在这里,我们提出了一种简单但通用的方法,用于对纳升级生物样品进行几乎无损的样品调理和制备,使样品保持在接近生理条件下。用微毛细管吸取 3-5 纳升的样品。将微毛细管尖端浸入负染色或海藻糖的储液器中,样品通过盐和重金属离子或糖分子的扩散交换分别进行调理,然后将其作为小斑点沉积在 EM 网格上。我们展示了该方法在透射 EM 成像中用于制备蛋白质颗粒,以及在电子衍射分析中用于制备纳米晶体的用途。此外,该方法所需的微小样品体积可实现替代的生物实验策略,例如通过可视化蛋白质组学分析单个细胞的内容,充分利用 EM 的单分子检测极限。