Departments of Biological Chemistry and Physiology, University of California, Los Angeles, CA, USA.
IUCrJ. 2023 Jul 1;10(Pt 4):430-436. doi: 10.1107/S2052252523004141.
In this work, a novel crystal growth method termed suspended drop crystallization has been developed. Unlike traditional methods, this technique involves mixing protein and precipitant directly on an electron microscopy grid without any additional support layers. The grid is then suspended within a crystallization chamber designed in-house, allowing for vapor diffusion to occur from both sides of the drop. A UV-transparent window above and below the grid enables the monitoring of crystal growth via light, UV or fluorescence microscopy. Once crystals have formed, the grid can be removed and utilized for X-ray crystallography or microcrystal electron diffraction (MicroED) directly without having to manipulate the crystals. To demonstrate the efficacy of this method, crystals of the enzyme proteinase K were grown and its structure was determined by MicroED following focused ion beam/scanning electron microscopy milling to render the sample thin enough for cryoEM. Suspended drop crystallization overcomes many of the challenges associated with sample preparation, providing an alternative workflow for crystals embedded in viscous media, sensitive to mechanical stress and/or subject to preferred orientation on electron microscopy grids.
在这项工作中,开发了一种称为悬滴结晶的新型晶体生长方法。与传统方法不同,该技术涉及在电子显微镜网格上直接混合蛋白质和沉淀剂,而无需任何其他支撑层。然后,网格悬挂在内部设计的结晶室内,允许从悬滴的两侧发生蒸汽扩散。网格上方和下方的 UV 透明窗允许通过光、紫外线或荧光显微镜监测晶体生长。一旦晶体形成,网格可以直接用于 X 射线晶体学或微晶体电子衍射(MicroED),而无需对晶体进行操作。为了证明该方法的有效性,生长了蛋白酶 K 酶蛋白的晶体,并通过聚焦离子束/扫描电子显微镜铣削来确定其结构,以使样品足够薄以进行 cryoEM。悬滴结晶克服了与样品制备相关的许多挑战,为嵌入粘性介质中的晶体提供了一种替代工作流程,这些晶体对机械应力敏感,并且/或者在电子显微镜网格上具有择优取向。