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8T9Z

Structural of M8C10 Fab in complex human metapneumovirus fusion protein

Summary for 8T9Z
Entry DOI10.2210/pdb8t9z/pdb
DescriptorFusion glycoprotein F0, M8C10 Fab Heavy Chain, M8C10 Fab Light Chain, ... (4 entities in total)
Functional Keywordsneutralizing antibody, respiratory, metapneumovirus, fusion, viral protein, viral protein-immune system complex, viral protein/immune system
Biological sourceHuman metapneumovirus
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Total number of polymer chains3
Total formula weight100125.63
Authors
Su, H.P.,Eddins, M.J.,Shipman, J.M.,Kostas, J.,Reid, J.C. (deposition date: 2023-06-26, release date: 2023-11-22, Last modification date: 2024-11-20)
Primary citationXiao, X.,Wen, Z.,Chen, Q.,Shipman, J.M.,Kostas, J.,Reid, J.C.,Warren, C.,Tang, A.,Luo, B.,O'Donnell, G.,Fridman, A.,Chen, Z.,Vora, K.A.,Zhang, L.,Su, H.-P.,Eddins, M.J.
Structural characterization of M8C10, a neutralizing antibody targeting a highly conserved prefusion-specific epitope on the metapneumovirus fusion trimerization interface.
J.Virol., 97:e0105223-e0105223, 2023
Cited by
PubMed Abstract: Human metapneumovirus (hMPV) is a common pathogen causing lower respiratory tract infections worldwide and can develop severe symptoms in high-risk populations such as infants, the elderly, and immunocompromised patients. There are no approved hMPV vaccines or neutralizing antibodies available for therapeutic or prophylactic use. The trimeric hMPV fusion F protein is the major target of neutralizing antibodies in human sera. Understanding the immune recognition of antibodies to hMPV-F antigen will provide critical insights into developing efficacious hMPV monoclonal antibodies and vaccines.
PubMed: 38032197
DOI: 10.1128/jvi.01052-23
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.995 Å)
Structure validation

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