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Table 2 Recombinant proteins produced in BEV for the development of COVID-19 vaccines

From: Application of Baculovirus Expression Vector system (BEV) for COVID-19 diagnostics and therapeutics: a review

Proteins

Modifications

Host Cells

Purification Method

Yield

Purity

Specific Applications

References

Spike protein, S1 and receptor-binding domain (RBD)

Signal peptide, ectodomain, T4 foldon trimerization domain, thrombin cleavage site, spacer, ferritin, viral protein, and peptide tags added. Mutations introduced to the sequences.

Sf9/Sf21/High Five/ expresSF+/ BmN/silkworm larvae

Affinity or anion or gel filtration chromatography/ Ultrasonic crushing and ultracentrifugation/ Tangential flow filtration/Dialysis

0.19 - 30 mg/l

90 - 98%

Subunit vaccine

[16, 19, 55,56,57,58,59]

Spike protein, S1, receptor binding domain (RBD)

Codon-optimized and fusion with MERS-CoV S gene corresponding to the N-terminal domain (NTD) (RBD).

Sf9/293T

Not applicable

Not applicable

Not applicable

DNA Vaccine

[60]

Envelope, Membrane, Spike, S1 and influenza matrix protein 1 proteins

Signal peptides, prefusion stabilized ectodomain, T4 fibritin  trimerization signal, peptide tags, linker, cleavage site, transmembrane and tail domain added. Codon optimization.

Sf9/ExpiSf9

Affinity chromatography/Sucrose gradient centrifugation

0.005 – 11 mg/mL

Not measured

VLP vaccine

[61,62,63]

Human angiotensin converting enzyme 2 (hACE2)

GP67 signal peptide sequence added at N terminus. Hexa-His tag added to the C terminus.

Sf9/High Five

Gel Filtration Chromatography

Not measured

Not measured

Surface plasmon resonance (SPR) assay

[64]