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Rotten to the core: antivirals targeting the HIV-1 capsid core
The capsid core of HIV-1 is a large macromolecular assembly that surrounds the viral genome and is an essential component of the infectious virus. In addition to its multiple roles throughout the viral life cycle, the capsid interacts with multiple host factors. Owing to its indispensable nature, th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693499/ https://www.ncbi.nlm.nih.gov/pubmed/34937567 http://dx.doi.org/10.1186/s12977-021-00583-z |
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author | McFadden, William M. Snyder, Alexa A. Kirby, Karen A. Tedbury, Philip R. Raj, Monika Wang, Zhengqiang Sarafianos, Stefan G. |
author_facet | McFadden, William M. Snyder, Alexa A. Kirby, Karen A. Tedbury, Philip R. Raj, Monika Wang, Zhengqiang Sarafianos, Stefan G. |
author_sort | McFadden, William M. |
collection | PubMed |
description | The capsid core of HIV-1 is a large macromolecular assembly that surrounds the viral genome and is an essential component of the infectious virus. In addition to its multiple roles throughout the viral life cycle, the capsid interacts with multiple host factors. Owing to its indispensable nature, the HIV-1 capsid has been the target of numerous antiretrovirals, though most capsid-targeting molecules have not had clinical success until recently. Lenacapavir, a long-acting drug that targets the HIV-1 capsid, is currently undergoing phase 2/3 clinical trials, making it the most successful capsid inhibitor to-date. In this review, we detail the role of the HIV-1 capsid protein in the virus life cycle, categorize antiviral compounds based on their targeting of five sites within the HIV-1 capsid, and discuss their molecular interactions and mechanisms of action. The diverse range of inhibition mechanisms provides insight into possible new strategies for designing novel HIV-1 drugs and furthers our understanding of HIV-1 biology. [Image: see text] |
format | Online Article Text |
id | pubmed-8693499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-86934992021-12-23 Rotten to the core: antivirals targeting the HIV-1 capsid core McFadden, William M. Snyder, Alexa A. Kirby, Karen A. Tedbury, Philip R. Raj, Monika Wang, Zhengqiang Sarafianos, Stefan G. Retrovirology Review The capsid core of HIV-1 is a large macromolecular assembly that surrounds the viral genome and is an essential component of the infectious virus. In addition to its multiple roles throughout the viral life cycle, the capsid interacts with multiple host factors. Owing to its indispensable nature, the HIV-1 capsid has been the target of numerous antiretrovirals, though most capsid-targeting molecules have not had clinical success until recently. Lenacapavir, a long-acting drug that targets the HIV-1 capsid, is currently undergoing phase 2/3 clinical trials, making it the most successful capsid inhibitor to-date. In this review, we detail the role of the HIV-1 capsid protein in the virus life cycle, categorize antiviral compounds based on their targeting of five sites within the HIV-1 capsid, and discuss their molecular interactions and mechanisms of action. The diverse range of inhibition mechanisms provides insight into possible new strategies for designing novel HIV-1 drugs and furthers our understanding of HIV-1 biology. [Image: see text] BioMed Central 2021-12-22 /pmc/articles/PMC8693499/ /pubmed/34937567 http://dx.doi.org/10.1186/s12977-021-00583-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review McFadden, William M. Snyder, Alexa A. Kirby, Karen A. Tedbury, Philip R. Raj, Monika Wang, Zhengqiang Sarafianos, Stefan G. Rotten to the core: antivirals targeting the HIV-1 capsid core |
title | Rotten to the core: antivirals targeting the HIV-1 capsid core |
title_full | Rotten to the core: antivirals targeting the HIV-1 capsid core |
title_fullStr | Rotten to the core: antivirals targeting the HIV-1 capsid core |
title_full_unstemmed | Rotten to the core: antivirals targeting the HIV-1 capsid core |
title_short | Rotten to the core: antivirals targeting the HIV-1 capsid core |
title_sort | rotten to the core: antivirals targeting the hiv-1 capsid core |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8693499/ https://www.ncbi.nlm.nih.gov/pubmed/34937567 http://dx.doi.org/10.1186/s12977-021-00583-z |
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