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蛋白质和病毒衣壳的相干衍射成像:模拟 MS SPIDOC。

Coherent diffractive imaging of proteins and viral capsids: simulating MS SPIDOC.

机构信息

Centre for Structural Systems Biology (CSSB), Deutsches Elektronen-Synchrotron DESY, Notkestraße 85, 22607, Hamburg, Germany.

Leibniz Institute of Virology (LIV), Martinistraße 52, 20251, Hamburg, Germany.

出版信息

Anal Bioanal Chem. 2023 Jul;415(18):4209-4220. doi: 10.1007/s00216-023-04658-y. Epub 2023 Apr 4.

Abstract

MS SPIDOC is a novel sample delivery system designed for single (isolated) particle imaging at X-ray Free-Electron Lasers that is adaptable towards most large-scale facility beamlines. Biological samples can range from small proteins to MDa particles. Following nano-electrospray ionization, ionic samples can be m/z-filtered and structurally separated before being oriented at the interaction zone. Here, we present the simulation package developed alongside this prototype. The first part describes how the front-to-end ion trajectory simulations have been conducted. Highlighted is a quadrant lens; a simple but efficient device that steers the ion beam within the vicinity of the strong DC orientation field in the interaction zone to ensure spatial overlap with the X-rays. The second part focuses on protein orientation and discusses its potential with respect to diffractive imaging methods. Last, coherent diffractive imaging of prototypical T = 1 and T = 3 norovirus capsids is shown. We use realistic experimental parameters from the SPB/SFX instrument at the European XFEL to demonstrate that low-resolution diffractive imaging data (q < 0.3 nm) can be collected with only a few X-ray pulses. Such low-resolution data are sufficient to distinguish between both symmetries of the capsids, allowing to probe low abundant species in a beam if MS SPIDOC is used as sample delivery.

摘要

MS SPIDOC 是一种新颖的样品输送系统,专为 X 射线自由电子激光的单(孤立)颗粒成像而设计,可适应大多数大规模设施光束线。生物样品的范围可以从小的蛋白质到大分子量的颗粒。在纳米电喷雾电离之后,可以对离子样品进行 m/z 过滤和结构分离,然后在相互作用区域定向。在这里,我们展示了与该原型一起开发的模拟软件包。第一部分描述了如何进行从头到尾的离子轨迹模拟。重点介绍了四象限透镜;这是一种简单但高效的装置,它可以在相互作用区域中的强直流取向场附近引导离子束,以确保与 X 射线的空间重叠。第二部分侧重于蛋白质的取向,并讨论了其相对于衍射成像方法的潜力。最后,展示了典型的 T = 1 和 T = 3 诺如病毒衣壳的相干衍射成像。我们使用欧洲 XFEL 的 SPB/SFX 仪器的实际实验参数来证明,仅使用几个 X 射线脉冲就可以收集低分辨率衍射成像数据(q < 0.3nm)。这种低分辨率数据足以区分衣壳的两种对称性,如果使用 MS SPIDOC 作为样品输送,则可以探测光束中的低丰度物质。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5702/10329076/173e1adef01d/216_2023_4658_Fig1_HTML.jpg

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