tetano
Editor, Senior Moderator
PLoS Pathog
. 2026 Aug 3;22(8):e1014391.
doi: 10.1371/journal.ppat.1014391. eCollection 2026 Aug.
Structural and functional characterization of a conserved cryptic epitope on SARS-CoV-2 spike S2 subunit
Ling Zhou[SUP] 1 [/SUP], Ching-Lin Hsieh[SUP] 1 [/SUP], Sarah R Leist[SUP] 2 [/SUP], Emily Happy Miller[SUP] 3 4 [/SUP], Andrew P Horton[SUP] 5 [/SUP], Sophie R Shoemaker[SUP] 6 [/SUP], Elizabeth C Gardner[SUP] 1 [/SUP], John M Powers[SUP] 2 [/SUP], Daniel R Boutz[SUP] 5 [/SUP], Michael L Mallory[SUP] 2 [/SUP], Connor M Mullins[SUP] 1 [/SUP], Nicole V Johnson[SUP] 1 [/SUP], Alexandra L Tse[SUP] 3 [/SUP], Albert Wang[SUP] 3 [/SUP], Kamyab Javanmardi[SUP] 1 [/SUP], Lily E Adams[SUP] 2 [/SUP], Jonathan Schisler[SUP] 7 8 9 [/SUP], Susan Marqusee[SUP] 6 10 11 12 [/SUP], Kartik Chandran[SUP] 3 [/SUP], Ralph S Baric[SUP] 2 [/SUP], Jimmy D Gollihar[SUP] 5 [/SUP], Jason S McLellan[SUP] 1 [/SUP]
Affiliations
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has undergone extensive evolution since its emergence in 2019, underscoring the continuous need for vaccines and therapeutics effective against multiple variants of concern (VOCs). The S2 subunit of the viral spike (S) glycoprotein is highly conserved among sarbecoviruses, making it an attractive target for broadly protective countermeasures. To elucidate the S2 antigenic landscape, we employed yeast surface display to isolate S2-targeted antibodies from COVID-19 convalescent donors. Biophysical characterization revealed that these S2 apex-directed antibodies preferentially bind to open spike conformations and a stabilized S2 construct but not to the closed, trimeric prefusion spike. Cryo-electron microscopy structures defined a cryptic epitope encompassing the upper helix and fusion peptide proximal region on S2. This epitope is conserved among sarbecoviruses but remains largely occluded in the closed prefusion conformation of the spikes. As a result, the antibodies exhibited weak neutralization activity against SARS-CoV-2 pseudoviruses, failed to neutralize authentic viruses, and did not provide protection in a lethal mouse challenge model using a mouse-adapted SARS-CoV-2 strain. These findings highlight a non-neutralizing epitope on S2 capable of eliciting antibodies during SARS-CoV-2 infection in humans and provide valuable reagents for probing S2 conformational dynamics and optimizing S2-based vaccine antigens.
. 2026 Aug 3;22(8):e1014391.
doi: 10.1371/journal.ppat.1014391. eCollection 2026 Aug.
Structural and functional characterization of a conserved cryptic epitope on SARS-CoV-2 spike S2 subunit
Ling Zhou[SUP] 1 [/SUP], Ching-Lin Hsieh[SUP] 1 [/SUP], Sarah R Leist[SUP] 2 [/SUP], Emily Happy Miller[SUP] 3 4 [/SUP], Andrew P Horton[SUP] 5 [/SUP], Sophie R Shoemaker[SUP] 6 [/SUP], Elizabeth C Gardner[SUP] 1 [/SUP], John M Powers[SUP] 2 [/SUP], Daniel R Boutz[SUP] 5 [/SUP], Michael L Mallory[SUP] 2 [/SUP], Connor M Mullins[SUP] 1 [/SUP], Nicole V Johnson[SUP] 1 [/SUP], Alexandra L Tse[SUP] 3 [/SUP], Albert Wang[SUP] 3 [/SUP], Kamyab Javanmardi[SUP] 1 [/SUP], Lily E Adams[SUP] 2 [/SUP], Jonathan Schisler[SUP] 7 8 9 [/SUP], Susan Marqusee[SUP] 6 10 11 12 [/SUP], Kartik Chandran[SUP] 3 [/SUP], Ralph S Baric[SUP] 2 [/SUP], Jimmy D Gollihar[SUP] 5 [/SUP], Jason S McLellan[SUP] 1 [/SUP]
Affiliations
- PMID: 42546045
- DOI: 10.1371/journal.ppat.1014391
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) has undergone extensive evolution since its emergence in 2019, underscoring the continuous need for vaccines and therapeutics effective against multiple variants of concern (VOCs). The S2 subunit of the viral spike (S) glycoprotein is highly conserved among sarbecoviruses, making it an attractive target for broadly protective countermeasures. To elucidate the S2 antigenic landscape, we employed yeast surface display to isolate S2-targeted antibodies from COVID-19 convalescent donors. Biophysical characterization revealed that these S2 apex-directed antibodies preferentially bind to open spike conformations and a stabilized S2 construct but not to the closed, trimeric prefusion spike. Cryo-electron microscopy structures defined a cryptic epitope encompassing the upper helix and fusion peptide proximal region on S2. This epitope is conserved among sarbecoviruses but remains largely occluded in the closed prefusion conformation of the spikes. As a result, the antibodies exhibited weak neutralization activity against SARS-CoV-2 pseudoviruses, failed to neutralize authentic viruses, and did not provide protection in a lethal mouse challenge model using a mouse-adapted SARS-CoV-2 strain. These findings highlight a non-neutralizing epitope on S2 capable of eliciting antibodies during SARS-CoV-2 infection in humans and provide valuable reagents for probing S2 conformational dynamics and optimizing S2-based vaccine antigens.