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Structure determination of macromolecular complexes by cryo-electron microscopy in vitro and in situ

  • F. Förster*
  • , E. Villa
  • , D. Thomas
  • , A. Korinek
  • , W. Baumeister
  • *Corresponding author for this work

Research output: Chapter in Book/Report/Conference proceedingChapterAcademic

Abstract

Three-dimensional (3-D) cryo-electron microscopy (EM) comprises three different branches: single particle analysis (SPA), cryo-electron tomography (CET), and electron crystallography. In this introduction into 3-D cryo-EM we first summarize the principle of imaging frozen-hydrated specimens by a transmission electron microscope (TEM) three-dimensionally before giving an insight into state-of-the-art strategies for automated data acquisition. For SPA and CET, we then review the respective methodologies and some selected applications highlighting the potential of both techniques, and in less detail we summarize electron crystallography. Finally, we give an account of the rapidly developing methods for model building using cryo-EM maps.

Original languageEnglish
Title of host publicationComprehensive Biophysics
PublisherElsevier
Pages245-276
Number of pages32
Volume1
ISBN (Print)9780080957180
DOIs
Publication statusPublished - 2012
Externally publishedYes

Keywords

  • Chaperone
  • Cryo-electron microscopy
  • Cryo-electron tomography
  • Electron microscopy
  • Macromolecular complex
  • Modeling
  • Protease
  • Ribosome
  • Single-particle analysis
  • Structural biology

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