Direct visualization of HIV-1 with correlative live-cell microscopy and cryo-electron tomography

Structure. 2011 Nov 9;19(11):1573-81. doi: 10.1016/j.str.2011.09.006.

Abstract

Cryo-electron tomography (cryoET) allows 3D visualization of cellular structures at molecular resolution in a close-to-native state and therefore has the potential to help elucidate early events of HIV-1 infection in host cells. However, structural details of infecting HIV-1 have not been observed, due to technological challenges in working with rare and dynamic HIV-1 particles in human cells. Here, we report structural analysis of HIV-1 and host-cell interactions by means of a correlative high-speed 3D live-cell-imaging and cryoET method. Using this method, we showed under near-native conditions that intact hyperstable mutant HIV-1 cores are released into the cytoplasm of host cells. We further obtained direct evidence to suggest that a hyperstable mutant capsid, E45A, showed delayed capsid disassembly compared to the wild-type capsid. Together, these results demonstrate the advantages of our correlative live-cell and cryoET approach for imaging dynamic processes, such as viral infection.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Capsid Proteins / genetics
  • Capsid Proteins / metabolism
  • Cryoelectron Microscopy / instrumentation*
  • Cryoelectron Microscopy / methods
  • Electron Microscope Tomography / instrumentation*
  • Electron Microscope Tomography / methods
  • HIV Infections / virology*
  • HIV-1 / genetics
  • HIV-1 / physiology*
  • HeLa Cells
  • Host-Pathogen Interactions*
  • Human Immunodeficiency Virus Proteins / genetics
  • Human Immunodeficiency Virus Proteins / metabolism
  • Humans
  • Mutation, Missense
  • Single-Cell Analysis / methods
  • Virion / metabolism

Substances

  • Capsid Proteins
  • Human Immunodeficiency Virus Proteins