6ATT

39S Fab bound to HER2 ecd

Summary for 6ATT

• Entry DOI: 10.2210/pdb6att/pdb
• Descriptor: Receptor tyrosine-protein kinase erbB-2, Antibody 39S Fab heavy chain, Antibody 39S Fab light chain, ... (5 entities in total)
• Functional Keywords: antibody, fragment antigen binding, her2, receptor, immune system
• Biological source: Homo sapiens (Human); More
• Total number of polymer chains: 3
• Total formula weight: 118521.35

Authors

Oganesyan, V.Y.,Dall'Acqua, W.F. (deposition date: 2017-08-29, release date: 2018-04-25, Last modification date: 2024-10-09)

Primary citation

Oganesyan, V.,Peng, L.,Bee, J.S.,Li, J.,Perry, S.R.,Comer, F.,Xu, L.,Cook, K.,Senthil, K.,Clarke, L.,Rosenthal, K.,Gao, C.,Damschroder, M.,Wu, H.,Dall'Acqua, W.
Structural insights into the mechanism of action of a biparatopic anti-HER2 antibody.
J. Biol. Chem., 293:8439-8448, 2018

PubMed Abstract: Pathways of human epidermal growth factor (EGF) receptors are activated upon ligand-dependent or -independent homo- or heterodimerization and their subsequent transphosphorylation. Overexpression of these receptors positively correlates with transphosphorylation rates and increased tumor growth rates. MEDI4276, an anti-human epidermal growth factor receptor 2 (HER2) biparatopic antibody-drug conjugate, has two paratopes within each antibody arm. One, 39S, is aiming at the HER2 site involved in receptor dimerization and the second, single chain fragment (scFv), mimicking trastuzumab. Here we present the cocrystal structure of the 39S Fab-HER2 complex and, along with biophysical and functional assays, determine the corresponding epitope of MEDI4276 and its underlying mechanism of action. Our results reveal that MEDI4276's uniqueness is based first on the ability of its 39S paratope to block HER2 homo- or heterodimerization and second on its ability to cluster the receptors on the surface of receptor-overexpressing cells.

PubMed: 29669810
DOI: 10.1074/jbc.M117.818013

Experimental method

X-RAY DIFFRACTION (3.77 Å)