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A Structural Perspective of the Role of IP6 in Immature and Mature Retroviral Assembly

The small cellular molecule inositol hexakisphosphate (IP6) has been known for ~20 years to promote the in vitro assembly of HIV-1 into immature virus-like particles. However, the molecular details underlying this effect have been determined only recently, with the identification of the IP6 binding...

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Detalles Bibliográficos
Autores principales: Obr, Martin, Schur, Florian K. M., Dick, Robert A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473085/
https://www.ncbi.nlm.nih.gov/pubmed/34578434
http://dx.doi.org/10.3390/v13091853
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author Obr, Martin
Schur, Florian K. M.
Dick, Robert A.
author_facet Obr, Martin
Schur, Florian K. M.
Dick, Robert A.
author_sort Obr, Martin
collection PubMed
description The small cellular molecule inositol hexakisphosphate (IP6) has been known for ~20 years to promote the in vitro assembly of HIV-1 into immature virus-like particles. However, the molecular details underlying this effect have been determined only recently, with the identification of the IP6 binding site in the immature Gag lattice. IP6 also promotes formation of the mature capsid protein (CA) lattice via a second IP6 binding site, and enhances core stability, creating a favorable environment for reverse transcription. IP6 also enhances assembly of other retroviruses, from both the Lentivirus and the Alpharetrovirus genera. These findings suggest that IP6 may have a conserved function throughout the family Retroviridae. Here, we discuss the different steps in the viral life cycle that are influenced by IP6, and describe in detail how IP6 interacts with the immature and mature lattices of different retroviruses.
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spelling pubmed-84730852021-09-28 A Structural Perspective of the Role of IP6 in Immature and Mature Retroviral Assembly Obr, Martin Schur, Florian K. M. Dick, Robert A. Viruses Review The small cellular molecule inositol hexakisphosphate (IP6) has been known for ~20 years to promote the in vitro assembly of HIV-1 into immature virus-like particles. However, the molecular details underlying this effect have been determined only recently, with the identification of the IP6 binding site in the immature Gag lattice. IP6 also promotes formation of the mature capsid protein (CA) lattice via a second IP6 binding site, and enhances core stability, creating a favorable environment for reverse transcription. IP6 also enhances assembly of other retroviruses, from both the Lentivirus and the Alpharetrovirus genera. These findings suggest that IP6 may have a conserved function throughout the family Retroviridae. Here, we discuss the different steps in the viral life cycle that are influenced by IP6, and describe in detail how IP6 interacts with the immature and mature lattices of different retroviruses. MDPI 2021-09-17 /pmc/articles/PMC8473085/ /pubmed/34578434 http://dx.doi.org/10.3390/v13091853 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Review
Obr, Martin
Schur, Florian K. M.
Dick, Robert A.
A Structural Perspective of the Role of IP6 in Immature and Mature Retroviral Assembly
title A Structural Perspective of the Role of IP6 in Immature and Mature Retroviral Assembly
title_full A Structural Perspective of the Role of IP6 in Immature and Mature Retroviral Assembly
title_fullStr A Structural Perspective of the Role of IP6 in Immature and Mature Retroviral Assembly
title_full_unstemmed A Structural Perspective of the Role of IP6 in Immature and Mature Retroviral Assembly
title_short A Structural Perspective of the Role of IP6 in Immature and Mature Retroviral Assembly
title_sort structural perspective of the role of ip6 in immature and mature retroviral assembly
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8473085/
https://www.ncbi.nlm.nih.gov/pubmed/34578434
http://dx.doi.org/10.3390/v13091853
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