Viscous-medium-based crystal support in a sample holder for fixed-target serial femtosecond crystallography

被引:23
|
作者
Lee, Keondo [1 ]
Lee, Donghyeon [1 ]
Baek, Sangwon [2 ]
Park, Jaehyun [3 ]
Lee, Sang Jae [3 ]
Park, Sehan [3 ]
Chung, Wan Kyun [1 ]
Lee, Jong-Lam [2 ]
Cho, Hyun-Soo [4 ]
Cho, Yunje [5 ]
Nam, Ki Hyun [5 ]
机构
[1] Pohang Univ Sci & Technol, Dept Mech Engn, Pohang, South Korea
[2] Pohang Univ Sci & Technol, Dept Mat Sci & Engn, Pohang, South Korea
[3] Pohang Univ Sci & Technol, Pohang Accelerator Lab, Pohang, South Korea
[4] Yonsei Univ, Dept Syst Biol, Seoul, South Korea
[5] Pohang Univ Sci & Technol, Dept Life Sci, Pohang, South Korea
基金
新加坡国家研究基金会;
关键词
serial femtosecond crystallography; sample delivery; fixed-target scanning; viscous media; X-RAY-DIFFRACTION; FREE-ELECTRON LASER; MILLISECOND CRYSTALLOGRAPHY; PROTEIN MICROCRYSTALS; DELIVERY; CHIP;
D O I
10.1107/S1600576720008663
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Serial femtosecond crystallography (SFX) enables the determination of the room-temperature crystal structure of macromolecules, as well as providing time-resolved molecular dynamics data in pump-probe experiments. Fixed-target SFX (FT-SFX) can minimize sample consumption and physical effects on crystals during sample delivery. In FT-SFX studies, having a sample holder that can stably fix crystal samples is one of the key elements required for efficient data collection. Hence, development of sample holders from new materials capable of supporting various crystal sizes and shapes may expand the applications of FT-SFX. Here, a viscous-media-based crystal support in a sample holder for FT-SFX is introduced. Crystal samples were embedded in viscous media, namely gelatin and agarose, which were enclosed in a polyimide film. In the vertically placed sample holder, 10-15%(w/v) viscous gelatin and 1-4%(w/v) agarose gel stably supported crystals between two polyimide films, thereby preventing the crystals from descending owing to gravity. Using this method, FT-SFX experiments were performed with glucose isomerase and lysozyme embedded in gelatin and agarose, respectively. The room-temperature crystal structures of glucose isomerase and lysozyme were successfully determined at 1.75 and 1.80 angstrom resolutions, respectively. The glucose isomerase and lysozyme diffraction analyses were not impeded by excessive background scattering from the viscous media. This method is useful for delivering crystal samples of various sizes and shapes in FT-SFX experiments.
引用
收藏
页码:1051 / 1059
页数:9
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