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用于串行飞秒晶体学的注射-转移系统组合

Combination of an inject-and-transfer system for serial femtosecond crystallography.

作者信息

Lee Keondo, Kim Jihan, Baek Sangwon, Park Jaehyun, Park Sehan, Lee Jong-Lam, Chung Wan Kyun, Cho Yunje, Nam Ki Hyun

机构信息

Department of Mechanical Engineering, Pohang University of Science and Technology, Pohang, Republic of Korea.

Department of Life Science, Pohang University of Science and Technology, Pohang, Republic of Korea.

出版信息

J Appl Crystallogr. 2022 Jul 5;55(Pt 4):813-822. doi: 10.1107/S1600576722005556. eCollection 2022 Aug 1.

Abstract

Serial femtosecond crystallography (SFX) enables the determination of room-temperature crystal structures of macromolecules with minimized radiation damage and provides time-resolved molecular dynamics by pump-probe or mix-and-inject experiments. In SFX, a variety of sample delivery methods with unique advantages have been developed and applied. The combination of existing sample delivery methods can enable a new approach to SFX data collection that combines the advantages of the individual methods. This study introduces a combined inject-and-transfer system (BITS) method for sample delivery in SFX experiments: a hybrid injection and fixed-target scanning method. BITS allows for solution samples to be reliably deposited on ultraviolet ozone (UVO)-treated polyimide films, at a minimum flow rate of 0.5 nl min, in both vertical and horizontal scanning modes. To utilize BITS in SFX experiments, lysozyme crystal samples were embedded in a viscous lard medium and injected at flow rates of 50-100 nl min through a syringe needle onto a UVO-treated polyimide film, which was mounted on a fixed-target scan stage. The crystal samples deposited on the film were raster scanned with an X-ray free electron laser using a motion stage in both horizontal and vertical directions. Using the BITS method, the room-temperature structure of lysozyme was successfully determined at a resolution of 2.1 Å, and thus BITS could be utilized in future SFX experiments.

摘要

串行飞秒晶体学(SFX)能够在辐射损伤最小化的情况下测定室温下的大分子晶体结构,并通过泵浦-探测或混合-注入实验提供时间分辨分子动力学信息。在SFX中,已经开发并应用了多种具有独特优势的样品输送方法。现有样品输送方法的组合可以实现一种新的SFX数据收集方法,该方法结合了各个方法的优点。本研究介绍了一种用于SFX实验中样品输送的组合注入-转移系统(BITS)方法:一种混合注入和固定靶扫描方法。BITS允许溶液样品以最低0.5 nl min的流速可靠地沉积在经紫外线臭氧(UVO)处理的聚酰亚胺薄膜上,适用于垂直和水平扫描模式。为了在SFX实验中使用BITS,将溶菌酶晶体样品嵌入粘性猪油介质中,并以50-100 nl min的流速通过注射器针头注射到安装在固定靶扫描台上的经UVO处理的聚酰亚胺薄膜上。使用运动平台在水平和垂直方向上用X射线自由电子激光对沉积在薄膜上的晶体样品进行光栅扫描。使用BITS方法成功地以2.1 Å的分辨率测定了溶菌酶的室温结构,因此BITS可用于未来的SFX实验。

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