Cryo-electron tomography: gaining insight into cellular processes by structural approaches

Curr Opin Struct Biol. 2011 Oct;21(5):670-7. doi: 10.1016/j.sbi.2011.07.004. Epub 2011 Aug 2.

Abstract

Visualization of cellular processes at a resolution of the individual protein should involve integrative and complementary approaches that can eventually draw realistic functional and cellular landscapes. Electron tomography of vitrified but otherwise unaltered cells emerges as a central method for three-dimensional reconstruction of cellular architecture at a resolution of 2-6 nm. While a combination of correlative light-based microscopy with cryo-electron tomography (cryo-ET) provides medium-resolution insight into pivotal cellular processes, fitting high-resolution structural approaches, for example, X-ray crystallography, into reconstructed macromolecular assemblies provides unprecedented information on native protein assemblies. Thus, cryo-ET bridges the resolution gap between cellular and structural biology. In this article, we focus on the study of eukaryotic cells and macromolecular complexes in a close-to-life-state. We discuss recent developments and structural findings enabling major strides to be made in understanding complex physiological functions.

Publication types

  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Animals
  • Cell Nucleus / chemistry
  • Cryoelectron Microscopy / methods*
  • Cytoplasm / chemistry
  • Electron Microscope Tomography / methods*
  • Eukaryotic Cells / chemistry
  • Eukaryotic Cells / ultrastructure*
  • Image Processing, Computer-Assisted
  • Microscopy, Fluorescence
  • Multiprotein Complexes / chemistry
  • Nuclear Pore / ultrastructure
  • Protein Conformation
  • Protein Structure, Tertiary

Substances

  • Multiprotein Complexes