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10.1016/j.virusres.2021.198305

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33482242!7817443!33482242
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suck abstract from ncbi


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pmid33482242      Virus+Res 2021 ; 295 (ä): 198305
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  • A stable platform for the production of virus-like particles pseudotyped with the severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) spike protein #MMPMID33482242
  • Roy S; Ghani K; de Campos-Lima PO; Caruso M
  • Virus Res 2021[Apr]; 295 (ä): 198305 PMID33482242show ga
  • In this study, we showed that a codon optimized version of the spike (S) protein of SARS-CoV-2 can migrate to the cell membrane. However, efficient production of Moloney murine leukemia (MLV) infectious viral particles was only achieved with stable expression of a shorter S version in C-terminal (DeltaS) in MLV Gag-pol expressing cells. As compared to transient transfections, this platform generated viruses with a 1000-fold higher titer. DeltaS was 15-times more efficiently incorporated into VLPs as compared to S, and that was not due to steric interference between the cytoplasmic tail and the MLV capsid, as similar differences were also observed with extracellular vesicles. The amount of DeltaS incorporated into VLPs released from producer cells was high and estimated at 1.25 mug/mL S2 equivalent (S is comprised of S1 and S2). The resulting VLPs could potentially be used alone or as a boost of other immunization strategies for COVID-19.
  • |COVID-19 Vaccines/*immunology[MESH]
  • |Cell Line[MESH]
  • |Humans[MESH]
  • |Moloney murine leukemia virus/genetics[MESH]
  • |SARS-CoV-2/immunology[MESH]
  • |Spike Glycoprotein, Coronavirus/*biosynthesis/genetics/immunology[MESH]
  • |Vaccines, Synthetic/immunology[MESH]


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