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利用SACLA的X射线自由电子激光对生物细胞和细胞器进行低温相干X射线衍射成像的样品制备

Specimen preparation for cryogenic coherent X-ray diffraction imaging of biological cells and cellular organelles by using the X-ray free-electron laser at SACLA.

作者信息

Kobayashi Amane, Sekiguchi Yuki, Oroguchi Tomotaka, Okajima Koji, Fukuda Asahi, Oide Mao, Yamamoto Masaki, Nakasako Masayoshi

机构信息

Department of Physics, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku-ku, Yokohama, Kanagawa 223-8522, Japan.

RIKEN SPring-8 Center, 1-1-1 Kouto, Sayo, Hyogo 679-5148, Japan.

出版信息

J Synchrotron Radiat. 2016 Jul;23(Pt 4):975-89. doi: 10.1107/S1600577516007736. Epub 2016 May 31.

DOI:10.1107/S1600577516007736
PMID:27359147
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5357008/
Abstract

Coherent X-ray diffraction imaging (CXDI) allows internal structures of biological cells and cellular organelles to be analyzed. CXDI experiments have been conducted at 66 K for frozen-hydrated biological specimens at the SPring-8 Angstrom Compact Free-Electron Laser facility (SACLA). In these cryogenic CXDI experiments using X-ray free-electron laser (XFEL) pulses, specimen particles dispersed on thin membranes of specimen disks are transferred into the vacuum chamber of a diffraction apparatus. Because focused single XFEL pulses destroy specimen particles at the atomic level, diffraction patterns are collected through raster scanning the specimen disks to provide fresh specimen particles in the irradiation area. The efficiency of diffraction data collection in cryogenic experiments depends on the quality of the prepared specimens. Here, detailed procedures for preparing frozen-hydrated biological specimens, particularly thin membranes and devices developed in our laboratory, are reported. In addition, the quality of the frozen-hydrated specimens are evaluated by analyzing the characteristics of the collected diffraction patterns. Based on the experimental results, the internal structures of the frozen-hydrated specimens and the future development for efficient diffraction data collection are discussed.

摘要

相干X射线衍射成像(CXDI)能够分析生物细胞和细胞器的内部结构。在SPring-8埃紧凑型自由电子激光设施(SACLA)上,已对冷冻水合生物标本在66 K下进行了CXDI实验。在这些使用X射线自由电子激光(XFEL)脉冲的低温CXDI实验中,分散在标本盘薄膜上的标本颗粒被转移到衍射仪的真空室中。由于聚焦的单个XFEL脉冲会在原子水平上破坏标本颗粒,因此通过对标本盘进行光栅扫描来收集衍射图案,以便在照射区域提供新鲜的标本颗粒。低温实验中衍射数据收集的效率取决于所制备标本的质量。在此,报告了制备冷冻水合生物标本的详细程序,特别是我们实验室开发的薄膜和装置。此外,通过分析所收集衍射图案的特征来评估冷冻水合标本的质量。基于实验结果,讨论了冷冻水合标本的内部结构以及高效衍射数据收集的未来发展。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a35/5357008/f58f27aa1261/s-23-00975-fig11.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a35/5357008/f58f27aa1261/s-23-00975-fig11.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a35/5357008/65fe64bb88bd/s-23-00975-fig1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a35/5357008/8cebe66b6772/s-23-00975-fig2.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a35/5357008/e53d2f9ec9d0/s-23-00975-fig7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a35/5357008/5f84d27e2a49/s-23-00975-fig8.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a35/5357008/b94cdc4d92fc/s-23-00975-fig9.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a35/5357008/afb117655e4e/s-23-00975-fig10.jpg
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