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Cone-shaped HIV-1 capsids are transported through intact nuclear pores
Human immunodeficiency virus (HIV-1) remains a major health threat. Viral capsid uncoating and nuclear import of the viral genome are critical for productive infection. The size of the HIV-1 capsid is generally believed to exceed the diameter of the nuclear pore complex (NPC), indicating that capsid...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cell Press
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895898/ https://www.ncbi.nlm.nih.gov/pubmed/33571428 http://dx.doi.org/10.1016/j.cell.2021.01.025 |
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author | Zila, Vojtech Margiotta, Erica Turoňová, Beata Müller, Thorsten G. Zimmerli, Christian E. Mattei, Simone Allegretti, Matteo Börner, Kathleen Rada, Jona Müller, Barbara Lusic, Marina Kräusslich, Hans-Georg Beck, Martin |
author_facet | Zila, Vojtech Margiotta, Erica Turoňová, Beata Müller, Thorsten G. Zimmerli, Christian E. Mattei, Simone Allegretti, Matteo Börner, Kathleen Rada, Jona Müller, Barbara Lusic, Marina Kräusslich, Hans-Georg Beck, Martin |
author_sort | Zila, Vojtech |
collection | PubMed |
description | Human immunodeficiency virus (HIV-1) remains a major health threat. Viral capsid uncoating and nuclear import of the viral genome are critical for productive infection. The size of the HIV-1 capsid is generally believed to exceed the diameter of the nuclear pore complex (NPC), indicating that capsid uncoating has to occur prior to nuclear import. Here, we combined correlative light and electron microscopy with subtomogram averaging to capture the structural status of reverse transcription-competent HIV-1 complexes in infected T cells. We demonstrated that the diameter of the NPC in cellulo is sufficient for the import of apparently intact, cone-shaped capsids. Subsequent to nuclear import, we detected disrupted and empty capsid fragments, indicating that uncoating of the replication complex occurs by breaking the capsid open, and not by disassembly into individual subunits. Our data directly visualize a key step in HIV-1 replication and enhance our mechanistic understanding of the viral life cycle. |
format | Online Article Text |
id | pubmed-7895898 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Cell Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-78958982021-03-02 Cone-shaped HIV-1 capsids are transported through intact nuclear pores Zila, Vojtech Margiotta, Erica Turoňová, Beata Müller, Thorsten G. Zimmerli, Christian E. Mattei, Simone Allegretti, Matteo Börner, Kathleen Rada, Jona Müller, Barbara Lusic, Marina Kräusslich, Hans-Georg Beck, Martin Cell Article Human immunodeficiency virus (HIV-1) remains a major health threat. Viral capsid uncoating and nuclear import of the viral genome are critical for productive infection. The size of the HIV-1 capsid is generally believed to exceed the diameter of the nuclear pore complex (NPC), indicating that capsid uncoating has to occur prior to nuclear import. Here, we combined correlative light and electron microscopy with subtomogram averaging to capture the structural status of reverse transcription-competent HIV-1 complexes in infected T cells. We demonstrated that the diameter of the NPC in cellulo is sufficient for the import of apparently intact, cone-shaped capsids. Subsequent to nuclear import, we detected disrupted and empty capsid fragments, indicating that uncoating of the replication complex occurs by breaking the capsid open, and not by disassembly into individual subunits. Our data directly visualize a key step in HIV-1 replication and enhance our mechanistic understanding of the viral life cycle. Cell Press 2021-02-18 /pmc/articles/PMC7895898/ /pubmed/33571428 http://dx.doi.org/10.1016/j.cell.2021.01.025 Text en © 2021 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Article Zila, Vojtech Margiotta, Erica Turoňová, Beata Müller, Thorsten G. Zimmerli, Christian E. Mattei, Simone Allegretti, Matteo Börner, Kathleen Rada, Jona Müller, Barbara Lusic, Marina Kräusslich, Hans-Georg Beck, Martin Cone-shaped HIV-1 capsids are transported through intact nuclear pores |
title | Cone-shaped HIV-1 capsids are transported through intact nuclear pores |
title_full | Cone-shaped HIV-1 capsids are transported through intact nuclear pores |
title_fullStr | Cone-shaped HIV-1 capsids are transported through intact nuclear pores |
title_full_unstemmed | Cone-shaped HIV-1 capsids are transported through intact nuclear pores |
title_short | Cone-shaped HIV-1 capsids are transported through intact nuclear pores |
title_sort | cone-shaped hiv-1 capsids are transported through intact nuclear pores |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7895898/ https://www.ncbi.nlm.nih.gov/pubmed/33571428 http://dx.doi.org/10.1016/j.cell.2021.01.025 |
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