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HIV-1 Envelope Conformation, Allostery, and Dynamics

The HIV-1 envelope glycoprotein (Env) mediates host cell fusion and is the primary target for HIV-1 vaccine design. The Env undergoes a series of functionally important conformational rearrangements upon engagement of its host cell receptor, CD4. As the sole target for broadly neutralizing antibodie...

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Detalles Bibliográficos
Autores principales: Bennett, Ashley Lauren, Henderson, Rory
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150877/
https://www.ncbi.nlm.nih.gov/pubmed/34067073
http://dx.doi.org/10.3390/v13050852
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author Bennett, Ashley Lauren
Henderson, Rory
author_facet Bennett, Ashley Lauren
Henderson, Rory
author_sort Bennett, Ashley Lauren
collection PubMed
description The HIV-1 envelope glycoprotein (Env) mediates host cell fusion and is the primary target for HIV-1 vaccine design. The Env undergoes a series of functionally important conformational rearrangements upon engagement of its host cell receptor, CD4. As the sole target for broadly neutralizing antibodies, our understanding of these transitions plays a critical role in vaccine immunogen design. Here, we review available experimental data interrogating the HIV-1 Env conformation and detail computational efforts aimed at delineating the series of conformational changes connecting these rearrangements. These studies have provided a structural mapping of prefusion closed, open, and transition intermediate structures, the allosteric elements controlling rearrangements, and state-to-state transition dynamics. The combination of these investigations and innovations in molecular modeling set the stage for advanced studies examining rearrangements at greater spatial and temporal resolution.
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spelling pubmed-81508772021-05-27 HIV-1 Envelope Conformation, Allostery, and Dynamics Bennett, Ashley Lauren Henderson, Rory Viruses Review The HIV-1 envelope glycoprotein (Env) mediates host cell fusion and is the primary target for HIV-1 vaccine design. The Env undergoes a series of functionally important conformational rearrangements upon engagement of its host cell receptor, CD4. As the sole target for broadly neutralizing antibodies, our understanding of these transitions plays a critical role in vaccine immunogen design. Here, we review available experimental data interrogating the HIV-1 Env conformation and detail computational efforts aimed at delineating the series of conformational changes connecting these rearrangements. These studies have provided a structural mapping of prefusion closed, open, and transition intermediate structures, the allosteric elements controlling rearrangements, and state-to-state transition dynamics. The combination of these investigations and innovations in molecular modeling set the stage for advanced studies examining rearrangements at greater spatial and temporal resolution. MDPI 2021-05-07 /pmc/articles/PMC8150877/ /pubmed/34067073 http://dx.doi.org/10.3390/v13050852 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
Bennett, Ashley Lauren
Henderson, Rory
HIV-1 Envelope Conformation, Allostery, and Dynamics
title HIV-1 Envelope Conformation, Allostery, and Dynamics
title_full HIV-1 Envelope Conformation, Allostery, and Dynamics
title_fullStr HIV-1 Envelope Conformation, Allostery, and Dynamics
title_full_unstemmed HIV-1 Envelope Conformation, Allostery, and Dynamics
title_short HIV-1 Envelope Conformation, Allostery, and Dynamics
title_sort hiv-1 envelope conformation, allostery, and dynamics
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8150877/
https://www.ncbi.nlm.nih.gov/pubmed/34067073
http://dx.doi.org/10.3390/v13050852
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