Interprotomer crosstalk in mosaic viral glycoprotein trimers provides insight into polyvalent immunogen co-assembly.

Interprotomer crosstalk in mosaic viral glycoprotein trimers provides insight into polyvalent immunogen co-assembly.

Publication date: Sep 22, 2025

SARS-CoV-2 variants have demonstrated the ability to evade immune responses, leading to waves of infection throughout the pandemic. In response, bivalent mRNA vaccines, encoding the original Wuhan-Hu-1 and emerging variants, were developed to display both spike antigens. To date, it has not been determined whether co-transfection and co-translation of different SARS-CoV-2 variants results in co-assembly of mosaic heterotrimer antigens and how this may affect trimer stability, dynamics, and antigenicity. Understanding whether such mosaic heterotrimers can form and their implications for antigen structure can provide important information to guide future polyvalent vaccine design where multiple variants of an antigen are co-formulated. To investigate this, we purified mosaic spike assemblies of both genetically close (Omicron BA. 2 and XBB) and distant (Omicron BA. 2 and Wuhan-Hu-1 G614) strains. We found that the stability and integrity of mosaic spike trimers were maintained without misfolding or aggregation. Glycosylation profiles likewise were preserved relative to the homotrimer counterparts. Hydrogen/deuterium-exchange mass spectrometry and biolayer-interferometry were used to investigate the mosaic spike dynamics and any impact on epitope presentation and receptor binding. The Omicron-XBB heterotrimer, sharing a common fusion subunit sequence, retained protomer-specific dynamics similar to the corresponding homotrimers in antigenically important regions. The Omicron-G614 heterotrimer, co-assembling from protomers of divergent fusion subunit sequences, likewise showed overall similar dynamics and conformations in the receptor-binding subunit compared to the homotrimers. However, the incorporation of the Wuhan-Hu-1 G614 protomer led to a stabilizing effect on the relatively unstable Omicron fusion subunit in the heterotrimer. These findings reveal structural dynamic crosstalk in mosaic trimers, suggesting a potential for enhanced immunogen display and important considerations to be aware of in the use of polyvalent nucleic acid vaccines.

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Concepts Keywords
Future Co
G614 Dynamics
Immunogen Fusion
Stabilizing G614
Viral Heterotrimer
Hu
Important
Mosaic
Omicron
Polyvalent
Spike
Subunit
Trimers
Variants
Wuhan

Semantics

Type Source Name
disease MESH infection
pathway REACTOME Translation
pathway REACTOME Reproduction
disease IDO host
disease IDO process
disease IDO infectivity
disease MESH coinfection
disease MESH COVID 19 pandemic
drug DRUGBANK Proline
disease IDO cell
pathway REACTOME Immune System
drug DRUGBANK Aspartame
disease IDO production
pathway REACTOME Digestion
disease IDO site
drug DRUGBANK Sulpiride
drug DRUGBANK Immune Globulin Human
disease MESH dissociation
disease MESH influenza
disease IDO nucleic acid
disease MESH superinfection
drug DRUGBANK Hexocyclium
disease IDO reagent
drug DRUGBANK Sodium lauryl sulfate
drug DRUGBANK Methylergometrine
drug DRUGBANK Tromethamine
drug DRUGBANK Imidazole
drug DRUGBANK Nitrogen
drug DRUGBANK Edetic Acid
drug DRUGBANK Biotin
disease IDO protein
drug DRUGBANK Ademetionine
drug DRUGBANK Urea
drug DRUGBANK Phosphate ion
drug DRUGBANK Formic Acid
drug DRUGBANK Ethanol
drug DRUGBANK Pepsin
drug DRUGBANK Flunarizine
drug DRUGBANK Esomeprazole
disease IDO assay
drug DRUGBANK Activated charcoal
drug DRUGBANK Copper
drug DRUGBANK Medical air
drug DRUGBANK Tretamine
disease MESH pneumonia
drug DRUGBANK Carboxyamidotriazole
drug DRUGBANK Guanosine
disease IDO pathogen
disease MESH Emergency
disease MESH breakthrough infection
drug DRUGBANK Spinosad

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