National Institutes of Health/National Institute of General Medical Sciences (NIH/NIGMS)
R01 GM134775
United States
Citation
Journal: Nat Struct Mol Biol / Year: 2020 Title: Subnanometer structures of HIV-1 envelope trimers on aldrithiol-2-inactivated virus particles. Authors: Ze Li / Wenwei Li / Maolin Lu / Julian Bess / Cara W Chao / Jason Gorman / Daniel S Terry / Baoshan Zhang / Tongqing Zhou / Scott C Blanchard / Peter D Kwong / Jeffrey D Lifson / Walther Mothes / Jun Liu / Abstract: The HIV-1 envelope glycoprotein (Env) trimer, composed of gp120 and gp41 subunits, mediates viral entry into cells. Recombinant Env trimers have been studied structurally, but characterization of Env ...The HIV-1 envelope glycoprotein (Env) trimer, composed of gp120 and gp41 subunits, mediates viral entry into cells. Recombinant Env trimers have been studied structurally, but characterization of Env embedded in intact virus membranes has been limited to low resolution. Here, we deploy cryo-electron tomography and subtomogram averaging to determine the structures of Env trimers on aldrithiol-2 (AT-2)-inactivated virions in ligand-free, antibody-bound and CD4-bound forms at subnanometer resolution. Tomographic reconstructions document molecular features consistent with high-resolution structures of engineered soluble and detergent-solubilized Env trimers. One of three conformational states previously predicted by smFRET was not observed by cryo-ET, potentially owing to AT-2 inactivation. We did observe Env trimers to open in situ in response to CD4 binding, with an outward movement of gp120-variable loops and an extension of a critical gp41 helix. Overall features of Env trimer embedded in AT-2-treated virions appear well-represented by current engineered trimers.
History
Deposition
Feb 19, 2020
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Header (metadata) release
Mar 18, 2020
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Map release
Jul 1, 2020
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Update
Aug 19, 2020
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Current status
Aug 19, 2020
Processing site: RCSB / Status: Released
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