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9MRZ

Structure of HCV broadly neutralizing antibody RM1-73

Summary for 9MRZ
Entry DOI10.2210/pdb9mrz/pdb
DescriptorRM1-73 Fab light chain, RM1-73 Fab heavy chain, SULFATE ION, ... (5 entities in total)
Functional Keywordsmonkey, immune system
Biological sourceMacaca mulatta (Rhesus monkey)
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Total number of polymer chains4
Total formula weight96307.04
Authors
Nguyen, T.K.Y.,Stanfield, R.L.,Wilson, I.A. (deposition date: 2025-01-09, release date: 2026-01-14, Last modification date: 2026-08-05)
Primary citationNguyen, Y.T.K.,Chen, F.,Giang, E.,Saha, S.,Ueno, L.A.,Chen, C.,Watson, C.T.,Tzarum, N.,Wilson, I.A.,Law, M.,Stanfield, R.L.
Structural and genetic signatures of two classes of HCV E2 neutralizing face antibodies from non-human primates immunized with a recombinant E1E2.
Npj Vaccines, 2026
Cited by
PubMed Abstract: Hepatitis C continues to be a significant public health problem despite advancements in antiviral therapeutics. To eliminate this disease, an effective vaccine against new infections and re-infections is needed. However, to date only one Hepatitis C virus (HCV) envelope protein (E1E2) immunogen, developed by Chiron Inc., has been tested in a Phase I clinical trial (ClinicalTrials.gov identifier NCT00500747). To establish a benchmark for elicitation of broadly neutralizing antibodies (bnAbs) by E1E2, we previously immunized non-human primates (NHPs) with this immunogen and isolated monoclonal nAbs that exhibit neutralization potency comparable to human nAbs. Here we show that NHP nAbs, encoded by germline genes IGHV1-138*01 and IGHV4-NL_5*01 (homologs of human IGHV1-69*10 and IGHV4-59*12, respectively), recognize a relatively conserved E2 region (neutralizing face) proximal to antigenic region 3 (AR3). These NHP AR3-targeting nAbs share highly similar binding modes to human AR3-targeting nAbs, suggesting a similarity in human and NHP immune responses to the same HCV immunogen.
PubMed: 42009696
DOI: 10.1038/s41541-026-01449-1
PDB entries with the same primary citation
Experimental method
X-RAY DIFFRACTION (2.03 Å)
Structure validation

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