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用于高分辨率、单颗粒冷冻电子显微镜的数据的采集、预处理和实时分析。

Collection, pre-processing and on-the-fly analysis of data for high-resolution, single-particle cryo-electron microscopy.

机构信息

The Astbury Biostructure Laboratory, Astbury Centre for Structural Molecular Biology, Faculty of Biological Sciences, University of Leeds, Leeds, UK.

The Harvard Cryo-Electron Microscopy Center for Structural Biology, Harvard Medical School, Boston, MA, USA.

出版信息

Nat Protoc. 2019 Jan;14(1):100-118. doi: 10.1038/s41596-018-0084-8.

Abstract

The dramatic growth in the use of cryo-electron microscopy (cryo-EM) to generate high-resolution structures of macromolecular complexes has changed the landscape of structural biology. The majority of structures deposited in the Electron Microscopy Data Bank (EMDB) at higher than 4-Å resolution were collected on Titan Krios microscopes. Although the pipeline for single-particle data collection is becoming routine, there is much variation in how sessions are set up. Furthermore, when collection is under way, there are a range of approaches for efficiently moving and pre-processing these data. Here, we present a standard operating procedure for single-particle data collection with Thermo Fisher Scientific EPU software, using the two most common direct electron detectors (the Thermo Fisher Scientific Falcon 3 (F3EC) and the Gatan K2), as well as a strategy for structuring these data to enable efficient pre-processing and on-the-fly monitoring of data collection. This protocol takes 3-6 h to set up a typical automated data collection session.

摘要

冷冻电子显微镜(cryo-EM)在生成大分子复合物高分辨率结构方面的应用呈爆炸式增长,改变了结构生物学的面貌。在电子显微镜数据银行(EMDB)中,分辨率高于 4Å 的结构大多数都是在 Titan Krios 显微镜上收集的。虽然单颗粒数据采集的流程已变得常规,但在设置方面仍存在很多差异。此外,在采集过程中,还有一系列方法可用于有效地移动和预处理这些数据。在这里,我们使用 Thermo Fisher Scientific EPU 软件,展示了使用两种最常见的直接电子探测器(Thermo Fisher Scientific Falcon 3(F3EC)和 Gatan K2)进行单颗粒数据采集的标准操作程序,以及一种用于对这些数据进行结构化的策略,以实现高效的预处理和实时监测数据采集。设置一个典型的自动化数据采集会话通常需要 3-6 小时。

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