基于原生质谱的单颗粒低温电镜样品制备筛选

P. D. Olinares, J. Kang, E. Llewellyn, C. Chiu, James Chen, B. Malone, R. Saecker, E. Campbell, S. Darst, B. Chait
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引用次数: 19

摘要

单粒子低温电子显微镜(cryo-EM)的最新进展已经能够以高分辨率确定许多蛋白质组件的结构,从而对其功能产生前所未有的见解。然而,尽管具有非凡的能力,冷冻电镜仍然是耗时和资源密集的。因此,在冗长的冷冻电镜分析之前,有一种快速评估和优化样品质量的方法是有益的。为此,我们开发了一种原生质谱(nMS)平台,可提供样品质量的快速反馈和高度精简的生化筛选。由于nMS能够对蛋白质复合物进行精确的质量分析,因此它非常适合于样品在EM网格上冷冻前的组成、完整性和均匀性的常规评估。我们展示了基于nms的平台的实用性,该平台利用样本细菌转录复合物的结构特征以及导致COVID-19大流行的SARS-CoV-2病毒的复制转录组装来促进冷冻电镜研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Native Mass Spectrometry-Based Screening for Optimal Sample Preparation in Single Particle Cryo-EM
Recent advances in single-particle cryogenic electron microscopy (cryo-EM) have enabled the structural determination of numerous protein assemblies at high resolution, yielding unprecedented insights into their function. However, despite its extraordinary capabilities, cryo-EM remains time-consuming and resource-intensive. It is therefore beneficial to have a means for rapidly assessing and optimizing the quality of samples prior to lengthy cryo-EM analyses. To do this, we have developed a native mass spectrometry (nMS) platform that provides rapid feedback on sample quality and highly streamlined biochemical screening. Because nMS enables accurate mass analysis of protein complexes, it is well suited to routine evaluation of the composition, integrity, and homogeneity of samples prior to their plunge-freezing on EM grids. We demonstrate the utility of our nMS-based platform for facilitating cryo-EM studies using structural characterizations of exemplar bacterial transcription complexes as well as the replication-transcription assembly from the SARS-CoV-2 virus that is responsible for the COVID-19 pandemic.
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