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. 2022 Aug 11;27(16):5119.
doi: 10.3390/molecules27165119.

Investigation of the N-Glycosylation of the SARS-CoV-2 S Protein Contained in VLPs Produced in Nicotiana benthamiana

Affiliations

Investigation of the N-Glycosylation of the SARS-CoV-2 S Protein Contained in VLPs Produced in Nicotiana benthamiana

Juliette Balieu et al. Molecules. .

Abstract

The emergence of the SARS-CoV-2 coronavirus pandemic in China in late 2019 led to the fast development of efficient therapeutics. Of the major structural proteins encoded by the SARS-CoV-2 genome, the SPIKE (S) protein has attracted considerable research interest because of the central role it plays in virus entry into host cells. Therefore, to date, most immunization strategies aim at inducing neutralizing antibodies against the surface viral S protein. The SARS-CoV-2 S protein is heavily glycosylated with 22 predicted N-glycosylation consensus sites as well as numerous mucin-type O-glycosylation sites. As a consequence, O- and N-glycosylations of this viral protein have received particular attention. Glycans N-linked to the S protein are mainly exposed at the surface and form a shield-masking specific epitope to escape the virus antigenic recognition. In this work, the N-glycosylation status of the S protein within virus-like particles (VLPs) produced in Nicotiana benthamiana (N. benthamiana) was investigated using a glycoproteomic approach. We show that 20 among the 22 predicted N-glycosylation sites are dominated by complex plant N-glycans and one carries oligomannoses. This suggests that the SARS-CoV-2 S protein produced in N. benthamiana adopts an overall 3D structure similar to that of recombinant homologues produced in mammalian cells.

Keywords: COVID; N-glycans; Nicotiana benthamiana; SPIKE; biologics; biopharmaceuticals; mass spectrometry; plant molecular farming; vaccine.

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Conflict of interest statement

G.P.L. declares that he is a named inventor on granted patent WO 29087391 A1 which describes the HyperTrans expression system and associated pEAQ vectors used for the expression of the SARS-CoV-2 S protein. The funders had no role in the design of the study, in the collection, analyses, or interpretation of data, in the writing of the manuscript, or in the decision to publish the results.

Figures

Figure 1
Figure 1
MALDI-TOF mass spectrum profile of [M+Na]+ molecular ions of permethylated N-glycans released from the SARS-CoV-2 S protein produced in N. benthamiana. Structures of main oligosaccharides are depicted. Each N-glycan has been drawn according to the international nomenclature [22]. Blue square: GlcNAc; green circle: Man; yellow circle: Gal; red triangle: Fuc and yellow star: Xyl. Linkages of monosaccharides to the core GlcNAc2Man3GlcNAc2 and linkage of the Lea terminal antennae are indicated. See legend of Figure 2 for nomenclature of plant N-linked glycans.
Figure 2
Figure 2
Oligomannoses, hybrid and complex glycans N-linked to the SARS-CoV-2 S protein produced in plants. Complex N-glycans are named according to the terminal glycan residues attached to Man3GlcNAc2 N-glycan sequence (i.e., M2XF stands for Man3(Xyl)(Fuc)GlcNAc2). Glycan isomers differing by their attachment of GlcNAc (Gn) or Lea epitopes on the two α-mannose arms of the core are represented with a bracket (GnMXF, LeaMXF and LeaGNXF). Each N-glycan has been drawn according to the international nomenclature [22]. Linkages of monosaccharides to the core GlcNAc2Man3GlcNAc2 and of the Lea antennae are indicated.
Figure 3
Figure 3
MS/MS spectra of (a) dicharged ion at m/z 1327.09 assigned to the peptide D228-R237 N-linked to Man-7, (b) dicharged ion at m/z 1041.44 assigned to the peptide V341-R346 N-linked to GnMXF and (c) dicharged ion at m/z 1296.54 assigned to the peptide V341-R346 N-linked to LeaGnXF. Structures of fragment ions are depicted. Each N-glycan has been drawn according to the international nomenclature [22]. Blue square: GlcNAc; green circle: Man; red triangle: Fuc; yellow circle: Gal and yellow star: Xyl.
Figure 3
Figure 3
MS/MS spectra of (a) dicharged ion at m/z 1327.09 assigned to the peptide D228-R237 N-linked to Man-7, (b) dicharged ion at m/z 1041.44 assigned to the peptide V341-R346 N-linked to GnMXF and (c) dicharged ion at m/z 1296.54 assigned to the peptide V341-R346 N-linked to LeaGnXF. Structures of fragment ions are depicted. Each N-glycan has been drawn according to the international nomenclature [22]. Blue square: GlcNAc; green circle: Man; red triangle: Fuc; yellow circle: Gal and yellow star: Xyl.
Figure 4
Figure 4
Distribution of main N-glycans on the 22 N-glycosylation consensus sites of the SARS-CoV-2 S protein produced in plants. Distribution of all N-glycans per glycosite are reported in Table S1. Blue square: GlcNAc; green circle: Man; red triangle: Fuc; yellow circle: Gal and yellow star: Xyl.

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References

    1. Akash K., Sharma A., Kumar D., Singh S.K., Gupta G., Chellappan D.K., Dua K., Nagraik R. Molecular aspects of Omicron, vaccine development, and recombinant strain XE: A review. J. Med. Virol. 2022:1–16. doi: 10.1002/jmv.27936. - DOI - PMC - PubMed
    1. Shajahan A., Supekar N.T., Gleinich A.S., Azadi P. Deducing the N- and O-glycosylation profile of the spike protein of novel coronavirus SARS-CoV-2. Glycobiology. 2020;30:981–988. doi: 10.1093/glycob/cwaa042. - DOI - PMC - PubMed
    1. Watanabe Y., Allen J.D., Wrapp D., McLellan J.S., Crispin M. Site-specific glycan analysis of the SARS-CoV-2 spike. Science. 2020;369:330–333. doi: 10.1126/science.abb9983. - DOI - PMC - PubMed
    1. Sanda M., Morrison L., Goldman R. N- and O-Glycosylation of the SARS-CoV-2 Spike Protein. Anal. Chem. 2021;93:2003–2009. doi: 10.1021/acs.analchem.0c03173. - DOI - PMC - PubMed
    1. Wang D., Zhou B., Keppel T.R., Solano M., Baudys J., Goldstein J., Finn M., Fan X., Chapman A., Bundy J., et al. N-glycosylation profiles of the SARS-CoV-2 spike D614G mutant and its ancestral protein characterized by advanced mass spectrometry. Sci. Rep. 2021;11:23561. doi: 10.1038/s41598-021-02904-w. - DOI - PMC - PubMed

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