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Octahedral small virus-like particles of dengue virus type 2
Open accessPreprint — published as 10.1128/jvi.01809-24 · Paper page
Abstract
Flavivirus envelope (E) and precursor M (prM) proteins, when ectopically expressed, assemble into empty, virus-like particles (VLPs). Cleavage of prM to M and loss of the pr fragment converts the VLPs from immature to mature particles, mimicking a similar maturation of authentic virions. Most of the VLPs obtained by prM-E expression are smaller than virions; early, low-resolution cryo-EM studies suggested a simple, 60-subunit, icosahedral organization. We describe here the cryo-EM structure of immature, small VLPs from dengue virus type 2 and show that they have octahedral rather than icosahedral symmetry. The asymmetric unit of the octahedral particle is an asymmetric trimer of prM-E heterodimers, just as it is on icosahedral immature virions; the full, octahedrally symmetric particle thus has 24 such asymmetric trimers, or 72 prM-E heterodimers in all. Cleavage of prM and release of pr generates ovoid, somewhat irregular, mature particles. Previous work has shown that mature smVLPs have fusion properties identical to those of virions, consistent with local, virion-like clustering of 36 E dimers on their surface. The cryo-EM structure and the properties of these VLPs described here relate directly to on-going efforts to use them as vaccine immunogens. IMPORTANCE: Ectopic expression of flavivirus envelope (E) and precursor M (prM) proteins leads to formation and secretion of empty, virus-like particles (VLPs), which are candidate, non-infectious, virion-like components of flavivirus vaccines. We show that the immature particles of a major class of VLPs -- “small VLPs” (smVLPs), which have smaller diameter than those of virion size, -- are octahedrally (rather than icosahedrally) symmetric, with the same clustering of prM and E, as asymmetric trimers of prM-E heterodimers, found on immature virions. Cleavage of prM and formation of mature, smVLPs yields somewhat irregular, ovoid particles. Design and characterization of VLPs as vaccine components will need to take these properties into account.
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Highly accurate protein structure prediction with AlphaFold
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Metadata
- Authors
- Johnson, A., Traian, M. D., Walsh, R. M., Jenni, S., & Harrison, S. C.
- Affiliations
- Harvard University (US)
- Boston Children's Hospital (US)
- Corresponding author
- Harrison, Stephen C.
- Venue
- Journal of Virology
- Publisher
- openRxiv
- Published
- 2024-10-18
- Volume
- 99
- Issue
- 2
- Pages
- e0180924-e0180924
- ISSN
- 0022-538X (ISSN-L)
- PMC
- PMC11853069
- OpenAlex
- W4405920988
- Cited by
- 9
- References
- 1
- Citations by year
- 2026: 4 · 2025: 5
- FWCI
- 3.73
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Virology (publishedVersion, cc-by)
- bioRxiv (Cold Spring Harbor Laboratory) (acceptedVersion, cc-by-nc-nd)
- PubMed Central (publishedVersion, cc-by)
- PubMed (publishedVersion)
- DOAJ (DOAJ: Directory of Open Access Journals) (submittedVersion, cc-by-sa)
- Funders
- Howard Hughes Medical Institute
- National Institutes of Health (CA-13202)
- National Cancer Institute (CA-13202, R01CA013202, R37CA013202)
- Topics
- Health Sciences › Medicine › Public Health, Environmental and Occupational Health › Mosquito-borne diseases and control
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Enzyme Structure and Function
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Structural Biology › Advanced Electron Microscopy Techniques and Applications
- Keywords
- dengue virus type 2, virus-like particles, octahedral symmetry, icosahedral symmetry, envelope protein, VLP assembly, flavivirus vaccines
- MeSH terms
- Animals, Dengue Virus, Humans, Viral Envelope Proteins, Virion, Virus Assembly, Cryoelectron Microscopy, Protein Multimerization
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