7S7I
Crystal structure of Fab in complex with MICA alpha3 domain
Summary for 7S7I
| Entry DOI | 10.2210/pdb7s7i/pdb |
| Descriptor | MHC class I chain-related protein A, Fab heavy chain, Fab light chain, ... (6 entities in total) |
| Functional Keywords | immunoglobulin, checkpoint, antibody, complex, immune system |
| Biological source | Homo sapiens (Human) More |
| Total number of polymer chains | 18 |
| Total formula weight | 359110.35 |
| Authors | |
| Primary citation | Hogan, J.M.,Lee, P.S.,Wong, S.C.,West, S.M.,Morishige, W.H.,Bee, C.,Tapia, G.C.,Rajpal, A.,Strop, P.,Dollinger, G. Residue-Level Characterization of Antibody Binding Epitopes Using Carbene Chemical Footprinting. Anal.Chem., 95:3922-3931, 2023 Cited by PubMed Abstract: Characterization of antibody binding epitopes is an important factor in therapeutic drug discovery, as the binding site determines and drives antibody pharmacology and pharmacokinetics. Here, we present a novel application of carbene chemical footprinting with mass spectrometry for identification of antibody binding epitopes at the single-residue level. Two different photoactivated diazirine reagents provide complementary labeling information allowing structural refinement of the antibody binding interface. We applied this technique to map the epitopes of multiple MICA and CTLA-4 antibodies and validated the findings with X-ray crystallography and yeast surface display epitope mapping. The characterized epitopes were used to understand biolayer interferometry-derived competitive binding results at the structural level. We show that carbene footprinting provides fast and high-resolution epitope information critical in the antibody selection process and enables mechanistic understanding of function to accelerate the drug discovery process. PubMed: 36791402DOI: 10.1021/acs.analchem.2c03091 PDB entries with the same primary citation |
| Experimental method | X-RAY DIFFRACTION (2.4 Å) |
Structure validation
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