26WC

Local refinement of the mpox virus A35R protein in complexed with 17H1 Fab

Summary for 26WC

• Entry DOI: 10.2210/pdb26wc/pdb
• EMDB information: 80928
• Descriptor: Protein OPG161, Variable domain of the 17H1 heavy chain, Variable domain of the 17H1 light chain (3 entities in total)
• Functional Keywords: immune complex, viral protein
• Biological source: Monkeypox virus; More
• Total number of polymer chains: 6
• Total formula weight: 91302.04

Authors

Xiao, Y.X.,He, M.Z. (deposition date: 2026-05-18, release date: 2026-07-22)

Primary citation

Bai, S.,Song, S.,Wang, X.,Xiao, Y.,Long, Y.,Wu, F.,Wang, F.,Fan, Z.,Xu, J.,He, M.,Lu, H.
Discovery and Structural Characterization of a Highly Protective Neutralizing Antibody Targeting the Mpox Virus A35R Protein.
MedComm (2020), 7:e70804-e70804, 2026

PubMed Abstract: The recent resurgence of the mpox virus (MPXV) has raised global health concerns due to its potential to cause severe illness in vulnerable populations. Targeting the extracellular enveloped virus (EEV) protein A35R is a promising strategy to restrict viral dissemination within the host. In this study, we combined mRNA-LNP immunization with the Beacon Optofluidic system to rapidly screen and isolate high-affinity monoclonal antibodies. One of these antibodies, 17H1, exhibited exceptional neutralization against authentic MPXV. Cryo-electron microscopy (Cryo-EM) analysis revealed that 17H1 binds to a specific epitope at the distal ends of the A35R dimer. The interaction is stabilized by a unique network of hydrogen bonds and salt bridges, particularly involving residue E120, distinguishing its binding mode from previously reported A35R antibodies. Furthermore, 17H1 exhibited complete protective efficacy against MPXV infection in vivo and significantly reduced pulmonary viral load and lung pathogenesis. These findings highlight 17H1 as a promising therapeutic candidate for novel mpox interventions.

PubMed: 42358411
DOI: 10.1002/mco2.70804

Experimental method

ELECTRON MICROSCOPY (3.63 Å)