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A unified framework for packing deformable and non-deformable subcellular structures in crowded cryo-electron tomogram simulation

机译:一种统一的框架用于在拥挤的低温电子断层图像模拟中包装可变形和不可变形的亚细胞结构

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摘要

Cryo-electron tomography (Cryo-ET), which was first proposed in 1970s, is now a popular and powerful imaging technique in the fields of life and medical sciences [1–3]. A series of two-dimensional images recorded by electron microscopes are collected to generate 3D reconstruction of macromolecules and then used to analyze the architecture of these structures. In traditional sample preparation process, due to the incompatibility with vacuum, water in sample cells tends to boil out and leads to unacceptable explosions. This seriously effected the efficiency of the sample preparation process and the accuracy of result data. In order to extract the cellular structure more accurately with higher resolution, cryo-electron tomography has emerged, which prepares samples at low temperatures and is able to record the cellular structure in a natural state [4].
机译:在20世纪70年代首次提出的冷冻电子断层扫描(Cryo-et)现在是生命和医学科学领域的流行和强大的成像技术[1-3]。收集由电子显微镜记录的一系列二维图像以产生大分子的3D重建,然后用于分析这些结构的架构。在传统样品制备过程中,由于与真空不相容,样品细胞中的水趋于沸腾并导致不可接受的爆炸。这严重实现了样品制备过程的效率和结果数据的准确性。为了用更高的分辨率更精确地提取细胞结构,出现了冷冻电子断层扫描,其在低温下制备样品,并且能够在天然状态下记录细胞结构[4]。

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