8EQA

Crystal structure of human anti-N1 neuraminidase 2H08 Fab

Summary for 8EQA

• Entry DOI: 10.2210/pdb8eqa/pdb
• Related: 8e6k
• Descriptor: 2H08 Fab light chain, 2H08 Fab heavy chain, ZINC ION, ... (4 entities in total)
• Functional Keywords: antibody, neuraminidase, h1n1, broad protection, pandemic, immune system
• Biological source: Homo sapiens (Human); More
• Total number of polymer chains: 4
• Total formula weight: 95142.85

Authors

Zhu, X.,Wilson, I.A. (deposition date: 2022-10-07, release date: 2023-08-09, Last modification date: 2023-08-23)

Primary citation

Hansen, L.,McMahon, M.,Turner, H.L.,Zhu, X.,Turner, J.S.,Ozorowski, G.,Stadlbauer, D.,Vahokoski, J.,Schmitz, A.J.,Rizk, A.A.,Alsoussi, W.B.,Strohmeier, S.,Yu, W.,Choreno-Parra, J.A.,Jimenez-Alvarez, L.,Cruz-Lagunas, A.,Zuniga, J.,Mudd, P.A.,Cox, R.J.,Wilson, I.A.,Ward, A.B.,Ellebedy, A.H.,Krammer, F.
Human anti-N1 monoclonal antibodies elicited by pandemic H1N1 virus infection broadly inhibit HxN1 viruses in vitro and in vivo.
Immunity, 56:1927-, 2023

PubMed Abstract: Neuraminidase (NA) is one of the two influenza virus surface glycoproteins, and antibodies that target it are an independent correlate of protection. However, our current understanding of NA antigenicity is incomplete. Here, we describe human monoclonal antibodies (mAbs) from a patient with a pandemic H1N1 virus infection in 2009. Two mAbs exhibited broad reactivity and inhibited NA enzyme activity of seasonal H1N1 viruses circulating before and after 2009, as well as viruses with avian or swine N1s. The mAbs provided robust protection from lethal challenge with human H1N1 and avian H5N1 viruses in mice, and both target an epitope on the lateral face of NA. In summary, we identified two broadly protective NA antibodies that share a novel epitope, inhibited NA activity, and provide protection against virus challenge in mice. Our work reaffirms that NA should be included as a target in future broadly protective or universal influenza virus vaccines.

PubMed: 37506693
DOI: 10.1016/j.immuni.2023.07.004

Experimental method

X-RAY DIFFRACTION (2.55 Å)