Abstract
Alphavirus-based vectors have received considerable attention in the fields of antigen (Ag) presentation, epitope mapping, vaccinology, and gene therapy (1-12), because of their relative ease of manipulation, purification to high titers, and ability to express large amounts of protein (13). Several members of the Alphavirus genus, including Sindbis virus (SIN), Semliki Forest virus, and Venezuelan equine encephalitis virus, have been modified genetically for use as viral expression vectors for foreign Ags (1, 3, 8, 13-17). SIN virions are comprised of an icosahedral nucleocapsid surrounded by a plasma-membrane- derived envelope containing two viral glycoproteins, E1 and E2 (18). The nucleocapsid contains a single stranded, positive (+) sense RNA gene of approx 11,700 nucleotides, which is capped and polyadenylated, and associated with 240 copies of the viral capsid protein.
Keywords
- Semliki Forest Virus
- Vector Particle
- Venezuelan Equine Encephalitis Virus
- Vector Replicon
- Poor Transfection Efficiency
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.
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Polo, J.M., Bergmann, C.C. (2000). Sindbis Virus-Based Vectors for the Study of Class I Antigen Presentation In Vitro and In Vivo. In: Solheim, J.C. (eds) Antigen Processing and Presentation Protocols. Methods in Molecular Biology, vol 156. Humana Press. https://doi.org/10.1385/1-59259-062-4:111
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DOI: https://doi.org/10.1385/1-59259-062-4:111
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