Protocol for live-cell fluorescence-guided cryoFIB-milling and electron cryo-tomography of virus-infected cells

STAR Protoc. 2022 Dec 16;3(4):101696. doi: 10.1016/j.xpro.2022.101696. Epub 2022 Sep 22.

Abstract

Here, we present a protocol for assessing virus-infected cells using electron cryo-tomography (cryoET). It includes the basic workflows of seeding cells, plunge-freezing, clipping, cryo-focused ion beam milling (cryoFIB-milling), and cryoET, as well as two optional modules: micropatterning and live-cell fluorescence microscopy. We use an A549 human cell line and the virus HAdV5-pIX-mcherry in this protocol, but the comprehensive workflow can be easily transferred to other cell types and different types of virus infection or treatment. For complete details on the use and execution of this protocol, please refer to Pfitzner et al. (2021).

Keywords: Cell biology; Cryo-EM; Microscopy; Molecular biology; Structural biology.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Line
  • Cryoelectron Microscopy / methods
  • Electron Microscope Tomography* / methods
  • Electrons*
  • Humans
  • Microscopy, Fluorescence / methods