Live-Cell Structural Biology to Solve Biological Mechanisms: The Case of the Exocyst

Structure. 2019 Jun 4;27(6):886-892. doi: 10.1016/j.str.2019.04.010. Epub 2019 May 23.

Abstract

Historically, structural biology has been largely centered on in vitro approaches as the dominant technique to obtain indispensable high-resolution data. In situ structural biology is now poised to contribute with high-precision observations in a near-physiological context. Mass spectrometry, electron tomography, and fluorescence microscopy are opening up new opportunities for structural analysis, including the study of the protein machinery in living cells. The complementarity between studies is increasingly used to reveal biologically significant observations. Here we compare two complementary studies addressing the mechanisms of vesicle tethering with in vitro and in situ approaches. Cryoelectron microscopy and live-cell imaging assisted by anchoring platforms team up to explore elusive mechanisms of exocytosis, showing directions of future research.

Keywords: Cryo-EM; Cryo-ET; exocyst; exocytosis; integrative structural biology; light microscopy; molecular mechanisms in membrane biology.

Publication types

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

MeSH terms

  • Cell Membrane / metabolism
  • Cell Membrane / ultrastructure*
  • Cryoelectron Microscopy / methods*
  • Cytoplasm / metabolism
  • Cytoplasm / ultrastructure*
  • Electron Microscope Tomography / methods*
  • Exocytosis*
  • Models, Molecular
  • Protein Conformation
  • Protein Multimerization
  • Protein Transport
  • Proteins / chemistry*
  • Proteins / metabolism

Substances

  • Proteins