7BH8
3H4-Fab HLA-E-VL9 co-complex
Summary for 7BH8
Entry DOI | 10.2210/pdb7bh8/pdb |
Descriptor | HLA class I histocompatibility antigen, alpha chain E, Beta-2-microglobulin, 3H4 Fab heavy chain, ... (8 entities in total) |
Functional Keywords | antibody fab fragment mhc class i molecule human leukocyte antigen e, immune system |
Biological source | Homo sapiens (Human) More |
Total number of polymer chains | 10 |
Total formula weight | 193890.30 |
Authors | Walters, L.C.,Rozbesky, D. (deposition date: 2021-01-10, release date: 2022-04-13, Last modification date: 2024-10-23) |
Primary citation | Li, D.,Brackenridge, S.,Walters, L.C.,Swanson, O.,Harlos, K.,Rozbesky, D.,Cain, D.W.,Wiehe, K.,Scearce, R.M.,Barr, M.,Mu, Z.,Parks, R.,Quastel, M.,Edwards, R.J.,Wang, Y.,Rountree, W.,Saunders, K.O.,Ferrari, G.,Borrow, P.,Jones, E.Y.,Alam, S.M.,Azoitei, M.L.,Gillespie, G.M.,McMichael, A.J.,Haynes, B.F. Mouse and human antibodies bind HLA-E-leader peptide complexes and enhance NK cell cytotoxicity. Commun Biol, 5:271-271, 2022 Cited by PubMed Abstract: The non-classical class Ib molecule human leukocyte antigen E (HLA-E) has limited polymorphism and can bind HLA class Ia leader peptides (VL9). HLA-E-VL9 complexes interact with the natural killer (NK) cell receptors NKG2A-C/CD94 and regulate NK cell-mediated cytotoxicity. Here we report the isolation of 3H4, a murine HLA-E-VL9-specific IgM antibody that enhances killing of HLA-E-VL9-expressing cells by an NKG2A NK cell line. Structural analysis reveal that 3H4 acts by preventing CD94/NKG2A docking on HLA-E-VL9. Upon in vitro maturation, an affinity-optimized IgG form of 3H4 showes enhanced NK killing of HLA-E-VL9-expressing cells. HLA-E-VL9-specific IgM antibodies similar in function to 3H4 are also isolated from naïve B cells of cytomegalovirus (CMV)-negative, healthy humans. Thus, HLA-E-VL9-targeting mouse and human antibodies isolated from the naïve B cell antibody pool have the capacity to enhance NK cell cytotoxicity. PubMed: 35347236DOI: 10.1038/s42003-022-03183-5 PDB entries with the same primary citation |
Experimental method | X-RAY DIFFRACTION (1.8 Å) |
Structure validation
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