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Author Notes:

Address correspondence to Paul Spearman, Email: Paul Spearman, paul.spearman@emory.edu or Elizabeth R. Wright, Email: erwrigh@emory.edu.

J.D.S. and J.E.H. contributed equally to this work.

We thank Jeannette Taylor of the Emory University Robert P. Apkarian Integrated Electron Microscopy Core for assistance and Fredrick Leon for help with image processing.

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Subjects:

Research Funding:

This work was supported in part by Emory University, Children's Healthcare of Atlanta, the Center for AIDS Research at Emory University (P30 AI050409), and the Georgia Research Alliance to E.R.W.; NSF grant 0923395 to E.R.W; the James B. Pendleton Charitable Trust to P.S. and E.R.W.; and public health service grants F32GM112517 to J.D.S and NIH AI058828 to P.S.

Children's Healthcare of Atlanta to . James B. Pendleton Charitable Trust to . HHS | National Institutes of Health (NIH) http://dx.doi.org/10.13039/100000002 F32GM112517 to . HHS | National Institutes of Health (NIH) http://dx.doi.org/10.13039/100000002 R01AI058828 to . National Science Foundation (NSF) http://dx.doi.org/10.13039/100000001 0923395 to . Emory University http://dx.doi.org/10.13039/100006939 to . Center for AIDS Research, Emory University (CFAR) http://dx.doi.org/10.13039/100008374 P30 AI050409 to . Georgia Research Alliance (GRA) http://dx.doi.org/10.13039/100008065.

Keywords:

  • Science & Technology
  • Life Sciences & Biomedicine
  • Virology
  • SIMPLEX-VIRUS 1
  • ELECTRON-MICROSCOPY
  • CRYOELECTRON TOMOGRAPHY
  • PARTICLE RELEASE
  • VIRAL GLYCOPROTEINS
  • INHIBITS HIV-1
  • VPU PROTEIN
  • IN-VIVO
  • BST-2/TETHERIN
  • RESTRICTION

Three-Dimensional Structural Characterization of HIV-1 Tethered to Human Cells

Journal Title:

Journal of Virology

Volume:

Volume 90, Number 3

Publisher:

, Pages 1507-1521

Type of Work:

Article | Final Publisher PDF

Abstract:

Tetherin (BST2, CD317, or HM1.24) is a host cellular restriction factor that prevents the release of enveloped viruses by mechanically linking virions to the plasma membrane. The precise arrangement of tetherin molecules at the plasma membrane site of HIV-1 assembly, budding, and restriction is not well understood. To gain insight into the biophysical mechanism underlying tetherin-mediated restriction of HIV-1, we utilized cryo-electron tomography (cryo-ET) to directly visualize HIV-1 virus-like particles (VLPs) and virions tethered to human cells in three dimensions (3D). Rod-like densities that we refer to as tethers were seen connecting HIV-1 virions to each other and to the plasma membrane. Native immunogold labeling showed tetherin molecules located on HIV-1 VLPs and virions in positions similar to those of the densities observed by cryo-ET. The location of the tethers with respect to the ordered immature Gag lattice or mature conical core was random. However, tethers were not uniformly distributed on the viral membrane but rather formed clusters at sites of contact with the cell or other virions. Chains of tethered HIV-1 virions often were arranged in a linear fashion, primarily as single chains and, to a lesser degree, as branched chains. Distance measurements support the extended tetherin model, in which the coiled-coil ectodomains are oriented perpendicular with respect to the viral and plasma membranes.

Copyright information:

© 2016, American Society for Microbiology.

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