7LUC
Cryo-EM structure of RSV preF bound by Fabs 32.4K and 01.4B
Summary for 7LUC
Entry DOI | 10.2210/pdb7luc/pdb |
EMDB information | 23520 |
Descriptor | Fusion glycoprotein F0, 01.4B Fab Heavy chain, 01.4B Fab Light chain, ... (5 entities in total) |
Functional Keywords | rsv, viral fusogen, fusion protein, antibody, immune system, immune system-viral protein complex, immune system/viral protein |
Biological source | Respiratory syncytial virus More |
Total number of polymer chains | 15 |
Total formula weight | 330223.85 |
Authors | Wrapp, D.,McLellan, J.S. (deposition date: 2021-02-22, release date: 2021-04-21, Last modification date: 2024-11-20) |
Primary citation | Mukhamedova, M.,Wrapp, D.,Shen, C.H.,Gilman, M.S.A.,Ruckwardt, T.J.,Schramm, C.A.,Ault, L.,Chang, L.,Derrien-Colemyn, A.,Lucas, S.A.M.,Ransier, A.,Darko, S.,Phung, E.,Wang, L.,Zhang, Y.,Rush, S.A.,Madan, B.,Stewart-Jones, G.B.E.,Costner, P.J.,Holman, L.A.,Hickman, S.P.,Berkowitz, N.M.,Doria-Rose, N.A.,Morabito, K.M.,DeKosky, B.J.,Gaudinski, M.R.,Chen, G.L.,Crank, M.C.,Misasi, J.,Sullivan, N.J.,Douek, D.C.,Kwong, P.D.,Graham, B.S.,McLellan, J.S.,Mascola, J.R. Vaccination with prefusion-stabilized respiratory syncytial virus fusion protein induces genetically and antigenically diverse antibody responses. Immunity, 54:769-780.e6, 2021 Cited by PubMed Abstract: An effective vaccine for respiratory syncytial virus (RSV) is an unrealized public health goal. A single dose of the prefusion-stabilized fusion (F) glycoprotein subunit vaccine (DS-Cav1) substantially increases serum-neutralizing activity in healthy adults. We sought to determine whether DS-Cav1 vaccination induces a repertoire mirroring the pre-existing diversity from natural infection or whether antibody lineages targeting specific epitopes predominate. We evaluated RSV F-specific B cell responses before and after vaccination in six participants using complementary B cell sequencing methodologies and identified 555 clonal lineages. DS-Cav1-induced lineages recognized the prefusion conformation of F (pre-F) and were genetically diverse. Expressed antibodies recognized all six antigenic sites on the pre-F trimer. We identified 34 public clonotypes, and structural analysis of two antibodies from a predominant clonotype revealed a common mode of recognition. Thus, vaccination with DS-Cav1 generates a diverse polyclonal response targeting the antigenic sites on pre-F, supporting the development and advanced testing of pre-F-based vaccines against RSV. PubMed: 33823129DOI: 10.1016/j.immuni.2021.03.004 PDB entries with the same primary citation |
Experimental method | ELECTRON MICROSCOPY (3.21 Å) |
Structure validation
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