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ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly

Polymerization of Gag on the inner leaflet of the plasma membrane drives the assembly of Human Immunodeficiency Virus 1 (HIV-1). Gag recruits components of the endosomal sorting complexes required for transport (ESCRT) to facilitate membrane fission and virion release. ESCRT assembly is initiated by...

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Autores principales: Ku, Pei-I, Bendjennat, Mourad, Ballew, Jeff, Landesman, Michael B., Saffarian, Saveez
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023924/
https://www.ncbi.nlm.nih.gov/pubmed/24834918
http://dx.doi.org/10.1371/journal.pone.0096950
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author Ku, Pei-I
Bendjennat, Mourad
Ballew, Jeff
Landesman, Michael B.
Saffarian, Saveez
author_facet Ku, Pei-I
Bendjennat, Mourad
Ballew, Jeff
Landesman, Michael B.
Saffarian, Saveez
author_sort Ku, Pei-I
collection PubMed
description Polymerization of Gag on the inner leaflet of the plasma membrane drives the assembly of Human Immunodeficiency Virus 1 (HIV-1). Gag recruits components of the endosomal sorting complexes required for transport (ESCRT) to facilitate membrane fission and virion release. ESCRT assembly is initiated by recruitment of ALIX and TSG101/ESCRT-I, which bind directly to the viral Gag protein and then recruit the downstream ESCRT-III and VPS4 factors to complete the budding process. In contrast to previous models, we show that ALIX is recruited transiently at the end of Gag assembly, and that most ALIX molecules are recycled into the cytosol as the virus buds, although a subset remains within the virion. Our experiments imply that ALIX is recruited to the neck of the assembling virion and is mostly recycled after virion release.
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spelling pubmed-40239242014-05-21 ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly Ku, Pei-I Bendjennat, Mourad Ballew, Jeff Landesman, Michael B. Saffarian, Saveez PLoS One Research Article Polymerization of Gag on the inner leaflet of the plasma membrane drives the assembly of Human Immunodeficiency Virus 1 (HIV-1). Gag recruits components of the endosomal sorting complexes required for transport (ESCRT) to facilitate membrane fission and virion release. ESCRT assembly is initiated by recruitment of ALIX and TSG101/ESCRT-I, which bind directly to the viral Gag protein and then recruit the downstream ESCRT-III and VPS4 factors to complete the budding process. In contrast to previous models, we show that ALIX is recruited transiently at the end of Gag assembly, and that most ALIX molecules are recycled into the cytosol as the virus buds, although a subset remains within the virion. Our experiments imply that ALIX is recruited to the neck of the assembling virion and is mostly recycled after virion release. Public Library of Science 2014-05-16 /pmc/articles/PMC4023924/ /pubmed/24834918 http://dx.doi.org/10.1371/journal.pone.0096950 Text en © 2014 Ku et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Ku, Pei-I
Bendjennat, Mourad
Ballew, Jeff
Landesman, Michael B.
Saffarian, Saveez
ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly
title ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly
title_full ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly
title_fullStr ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly
title_full_unstemmed ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly
title_short ALIX Is Recruited Temporarily into HIV-1 Budding Sites at the End of Gag Assembly
title_sort alix is recruited temporarily into hiv-1 budding sites at the end of gag assembly
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023924/
https://www.ncbi.nlm.nih.gov/pubmed/24834918
http://dx.doi.org/10.1371/journal.pone.0096950
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