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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...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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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. |
format | Online Article Text |
id | pubmed-8150877 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT bennettashleylauren hiv1envelopeconformationallosteryanddynamics AT hendersonrory hiv1envelopeconformationallosteryanddynamics |