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7S7I

Crystal structure of Fab in complex with MICA alpha3 domain

Summary for 7S7I
Entry DOI10.2210/pdb7s7i/pdb
DescriptorMHC class I chain-related protein A, Fab heavy chain, Fab light chain, ... (6 entities in total)
Functional Keywordsimmunoglobulin, checkpoint, antibody, complex, immune system
Biological sourceHomo sapiens (Human)
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Total number of polymer chains18
Total formula weight359110.35
Authors
Lee, P.S.,Strop, P. (deposition date: 2021-09-16, release date: 2022-10-05, Last modification date: 2024-11-13)
Primary citationHogan, 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: 36791402
DOI: 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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