Immunology
Structural insights into the mechanism of action of a biparatopic anti-HER2 antibody

https://doi.org/10.1074/jbc.M117.818013Get rights and content
Under a Creative Commons license
open access

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.

analytical ultracentrifugation
antibody
crystallography
epitope mapping
phosphorylation

Cited by (0)

This work was supported by MedImmune LLC. The authors declare that they have no conflicts of interest with the contents of this article.

This article contains Fig. S1.

The atomic coordinates and structure factors (code 6ATT) have been deposited in the Protein Data Bank (http://wwpdb.org/).

2

Present address: Palleon Pharmaceuticals, 266 Second Ave., Waltham, MA 02451.

3

Present address: MacroGenics, 9704 Medical Center Dr., Rockville, MD 20850.

4

Present address: Salubris Biotherapeutics, Inc., 45 W Watkins Mill Rd., Gaithersburg, MD 20878.

5

Present address: Agilis Biotherapeutics, 245 First St., Ste. 1800, Cambridge, MA 02142.