- EMDB-47587: Negative stain EM map of polyclonal serum from mouse immunized wi... -
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Entry
Database: EMDB / ID: EMD-47587
Title
Negative stain EM map of polyclonal serum from mouse immunized with MERS-CoV S-2P-T33_dn10 in complex with MERS S-2P
Map data
Negative stain EM map of polyclonal serum from mouse immunized with MERS-CoV S-2P-T33_dn10 in complex with MERS S-2P.
Sample
Complex: Immune complex 2 of prefusion MERS-CoV spike glycoprotein stabilized with 2P mutations with polyclonal Fabs from mice immunized with MERS-CoV S-2P-T33_dn10.
Keywords
Fab / serum / immune complex / MERS-S2P / VIRAL PROTEIN
Biological species
Mus musculus (house mouse)
Method
single particle reconstruction / negative staining / Resolution: 15.0 Å
National Institutes of Health/National Institute Of Allergy and Infectious Diseases (NIH/NIAID)
P01AI167966
United States
National Science Foundation (NSF, United States)
DGE-2140004
United States
Citation
Journal: Cell Rep / Year: 2024 Title: Protein nanoparticle vaccines induce potent neutralizing antibody responses against MERS-CoV. Authors: Cara W Chao / Kaitlin R Sprouse / Marcos C Miranda / Nicholas J Catanzaro / Miranda L Hubbard / Amin Addetia / Cameron Stewart / Jack T Brown / Annie Dosey / Adian Valdez / Rashmi ...Authors: Cara W Chao / Kaitlin R Sprouse / Marcos C Miranda / Nicholas J Catanzaro / Miranda L Hubbard / Amin Addetia / Cameron Stewart / Jack T Brown / Annie Dosey / Adian Valdez / Rashmi Ravichandran / Grace G Hendricks / Maggie Ahlrichs / Craig Dobbins / Alexis Hand / Jackson McGowan / Boston Simmons / Catherine Treichel / Isabelle Willoughby / Alexandra C Walls / Andrew T McGuire / Elizabeth M Leaf / Ralph S Baric / Alexandra Schäfer / David Veesler / Neil P King / Abstract: Middle East respiratory syndrome coronavirus (MERS-CoV) is a betacoronavirus that causes severe respiratory illness in humans. There are no licensed vaccines against MERS-CoV and only a few ...Middle East respiratory syndrome coronavirus (MERS-CoV) is a betacoronavirus that causes severe respiratory illness in humans. There are no licensed vaccines against MERS-CoV and only a few candidates in phase I clinical trials. Here, we develop MERS-CoV vaccines utilizing a computationally designed protein nanoparticle platform that has generated safe and immunogenic vaccines against various enveloped viruses, including a licensed vaccine for severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2). Two-component nanoparticles displaying spike (S)-derived antigens induce neutralizing responses and protect mice against challenge with mouse-adapted MERS-CoV. Epitope mapping reveals the dominant responses elicited by immunogens displaying the prefusion-stabilized S-2P trimer, receptor binding domain (RBD), or N-terminal domain (NTD). An RBD nanoparticle elicits antibodies targeting multiple non-overlapping epitopes in the RBD. Our findings demonstrate the potential of two-component nanoparticle vaccine candidates for MERS-CoV and suggest that this platform technology could be broadly applicable to betacoronavirus vaccine development.
Name: Immune complex 2 of prefusion MERS-CoV spike glycoprotein stabilized with 2P mutations with polyclonal Fabs from mice immunized with MERS-CoV S-2P-T33_dn10.
Components
Complex: Immune complex 2 of prefusion MERS-CoV spike glycoprotein stabilized with 2P mutations with polyclonal Fabs from mice immunized with MERS-CoV S-2P-T33_dn10.
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