4.6 Article

Utility of Alternative Promoters for Foreign Gene Expression Using the Baculovirus Expression Vector System

Journal

VIRUSES-BASEL
Volume 14, Issue 12, Pages -

Publisher

MDPI
DOI: 10.3390/v14122670

Keywords

promoters; baculovirus expression vector system; BEVS; virus-like particle; VLP; p6; 9; 39k; vp39; ctx; orf75; 38k; gp64

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Funding

  1. Natural Sciences and Engineering Research Council of Canada (NSERC) [RGPIN 355513-2017]
  2. Strategic Project Grants [STPGP 462995-14]

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The study identified promoters for optimizing the expression of foreign genes in the baculovirus expression vector system by using previously published transcriptome data, and used bioinformatics to determine sequence determinants that may be crucial for late gene transcription and translation initiation.
The baculovirus expression vector system (BEVS) is a widely used platform for recombinant protein production for use in a wide variety of applications. Of particular interest is production of virus-like particles (VLPs), which consist of multiple viral proteins that self-assemble in strict stoichiometric ratios to mimic the structure of a virus but lacks its genetic material, while a significant amount of effort has been spent on optimizing expression ratios by co-infecting cells with multiple recombinant BEVs and modulating different process parameters, co-expressing multiple foreign genes from a single rBEV may offer more promise. However, there is currently a lack of promoters available with which to optimize co-expression of each foreign gene. To address this, previously published transcriptome data was used to identify promoters that have incrementally lower expression profiles and compared by expressing model cytoplasmic and secreted proteins. Bioinformatics was also used to identify sequence determinants that may be important for late gene transcription regulation, and translation initiation. The identified promoters and bioinformatics analyses may be useful for optimizing expression of foreign genes in the BEVS.

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