Anaerobic fixed-target serial crystallography using sandwiched silicon nitride membranes.

IF 2.6 4区 生物学 Q2 BIOCHEMICAL RESEARCH METHODS
Monika Bjelčić, Kajsa G V Sigfridsson Clauss, Oskar Aurelius, Mirko Milas, Jie Nan, Thomas Ursby
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引用次数: 0

Abstract

In recent years, the emergence of serial crystallography, initially pioneered at X-ray free-electron lasers (XFELs), has sparked a growing interest in collecting macromolecular crystallographic data at room temperature. Various fixed-target serial crystallography techniques have been developed, ranging from commercially available chips to in-house designs implemented at different synchrotron facilities. Nevertheless, there is currently no commercially available chip (known to the authors) specifically designed for the direct handling of oxygen-sensitive samples. This study presents a methodology employing silicon nitride chips arranged in a `sandwich' configuration, enabling reliable room-temperature data collection from oxygen-sensitive samples. The method involves the utilization of a custom-made 3D-printed assembling tool and a MX sample holder. To validate the effectiveness of the proposed method, deoxyhemoglobin and methemoglobin samples were investigated using the BioMAX X-ray macromolecular crystallography beamline, the Balder X-ray absorption spectroscopy beamline and UV-Vis absorption spectroscopy.

使用夹层氮化硅膜的厌氧固定靶系列晶体学。
近年来,最初在X射线自由电子激光器(XFEL)上开创的系列晶体学的出现,引发了人们对在室温下收集大分子晶体学数据的兴趣。已经开发了各种固定目标系列结晶学技术,从商用芯片到在不同同步加速器设施中实现的内部设计。然而,目前还没有专门设计用于直接处理氧敏感样品的商用芯片(作者已知)。这项研究提出了一种方法,采用“三明治”配置的氮化硅芯片,能够从氧敏感样品中可靠地收集室温数据。该方法包括使用定制的3D打印组装工具和MX样品支架。为了验证所提出方法的有效性,使用BioMAX X射线大分子晶体学光束线、Balder X射线吸收光谱光束线和UV-Vis吸收光谱对脱氧血红蛋白和高铁血红蛋白样品进行了研究。
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来源期刊
Acta Crystallographica. Section D, Structural Biology
Acta Crystallographica. Section D, Structural Biology BIOCHEMICAL RESEARCH METHODSBIOCHEMISTRY &-BIOCHEMISTRY & MOLECULAR BIOLOGY
CiteScore
4.50
自引率
13.60%
发文量
216
期刊介绍: Acta Crystallographica Section D welcomes the submission of articles covering any aspect of structural biology, with a particular emphasis on the structures of biological macromolecules or the methods used to determine them. Reports on new structures of biological importance may address the smallest macromolecules to the largest complex molecular machines. These structures may have been determined using any structural biology technique including crystallography, NMR, cryoEM and/or other techniques. The key criterion is that such articles must present significant new insights into biological, chemical or medical sciences. The inclusion of complementary data that support the conclusions drawn from the structural studies (such as binding studies, mass spectrometry, enzyme assays, or analysis of mutants or other modified forms of biological macromolecule) is encouraged. Methods articles may include new approaches to any aspect of biological structure determination or structure analysis but will only be accepted where they focus on new methods that are demonstrated to be of general applicability and importance to structural biology. Articles describing particularly difficult problems in structural biology are also welcomed, if the analysis would provide useful insights to others facing similar problems.
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