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悬滴结晶法的设计与实现

Design and implementation of suspended drop crystallization.

作者信息

Gillman Cody, Nicolas William J, Martynowycz Michael W, Gonen Tamir

机构信息

Departments of Biological Chemistry and Physiology, University of California, Los Angeles CA, USA.

Molecular Biology Institute, University of California, Los Angeles, Los Angeles, CA 90095, USA.

出版信息

bioRxiv. 2023 Mar 28:2023.03.28.534639. doi: 10.1101/2023.03.28.534639.

Abstract

We have developed a novel crystal growth method known as suspended drop crystallization. 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 which we designed, 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, we grew crystals of the enzyme proteinase K and determined its structure by MicroED following FIB/SEM 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 suffering from preferred orientation on EM grids.

摘要

我们开发了一种名为悬滴结晶的新型晶体生长方法。与传统方法不同,该技术直接在电子显微镜网格上混合蛋白质和沉淀剂,无需任何额外的支撑层。然后将网格悬浮在我们设计的结晶室内,使液滴两侧都能发生蒸汽扩散。网格上方和下方的紫外线透明窗口能够通过光学、紫外线或荧光显微镜监测晶体生长。一旦晶体形成,网格可以直接取出并用于X射线晶体学或微晶电子衍射(MicroED),而无需对晶体进行操作。为了证明该方法的有效性,我们培养了蛋白酶K的晶体,并在进行聚焦离子束/扫描电子显微镜(FIB/SEM)研磨以使样品薄到足以进行冷冻电镜观察后,通过MicroED确定了其结构。悬滴结晶克服了许多与样品制备相关的挑战,为嵌入粘性介质、对机械应力敏感和/或在电子显微镜网格上存在择优取向的晶体提供了一种替代工作流程。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/425a/10081258/8d95cfb68812/nihpp-2023.03.28.534639v1-f0001.jpg

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