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Journal article
Structure, Function, and Interactions of the HIV-1 Capsid Protein
Life (Basel, Switzerland), v 11(2), pp 1-25
01 Feb 2021
PMID: 33572761
Featured in Collection : UN Sustainable Development Goals @ Drexel
Abstract
The capsid (CA) protein of the human immunodeficiency virus type 1 (HIV-1) is an essential structural component of a virion and facilitates many crucial life cycle steps through interactions with host cell factors. Capsid shields the reverse transcription complex from restriction factors while it enables trafficking to the nucleus by hijacking various adaptor proteins, such as FEZ1 and BICD2. In addition, the capsid facilitates the import and localization of the viral complex in the nucleus through interaction with NUP153, NUP358, TNPO3, and CPSF-6. In the later stages of the HIV-1 life cycle, CA plays an essential role in the maturation step as a constituent of the Gag polyprotein. In the final phase of maturation, Gag is cleaved, and CA is released, allowing for the assembly of CA into a fullerene cone, known as the capsid core. The fullerene cone consists of similar to*250 CA hexamers and 12 CA pentamers and encloses the viral genome and other essential viral proteins for the next round of infection. As research continues to elucidate the role of CA in the HIV-1 life cycle and the importance of the capsid protein becomes more apparent, CA displays potential as a therapeutic target for the development of HIV-1 inhibitors.
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Details
- Title
- Structure, Function, and Interactions of the HIV-1 Capsid Protein
- Creators
- Eric Rossi - Alliant TechsystemsMegan E. Meuser - Drexel UniversityCamille J. Cunanan - Drexel UniversitySimon Cocklin - Drexel University
- Publication Details
- Life (Basel, Switzerland), v 11(2), pp 1-25
- Publisher
- Mdpi
- Number of pages
- 25
- Grant note
- R01AI150491 / NIH/NIAID; United States Department of Health & Human Services; National Institutes of Health (NIH) - USA; NIH National Institute of Allergy & Infectious Diseases (NIAID)
- Resource Type
- Journal article
- Language
- English
- Academic Unit
- Biochemistry and Molecular Biology; Pharmacology and Physiology
- Web of Science ID
- WOS:000622709400001
- Scopus ID
- 2-s2.0-85100577205
- Other Identifier
- 991019167646304721
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Data related to this publication, from InCites Benchmarking & Analytics tool:
- Web of Science research areas
- Biology
- Microbiology