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Variants of the Antibody Herceptin That Interact with HER2 and VEGF at the Antigen Binding Site
Jenny Bostrom,1,2
Shang-Fan Yu,3
David Kan,3
Brent A. Appleton,1
Chingwei V. Lee,1,2
Karen Billeci,4
Wenyan Man,1
Franklin Peale,5
Sarajane Ross,3
Christian Wiesmann,1
Germaine Fuh1,2*
Abstract:
The interface between antibody and antigen is often depictedas a lock and key, suggesting that an antibody surface can accommodateonly one antigen. Here, we describe an antibody with an antigenbinding site that binds two distinct proteins with high affinity.We isolated a variant of Herceptin, a therapeutic monoclonalantibody that binds the human epidermal growth factor receptor2 (HER2), on the basis of its ability to simultaneously interactwith vascular endothelial growth factor (VEGF). Crystallographicand mutagenesis studies revealed that distinct amino acids ofthis antibody, called bH1, engage HER2 and VEGF energetically,but there is extensive overlap between the antibody surfaceareas contacting the two antigens. An affinity-improved versionof bH1 inhibits both HER2- and VEGF-mediated cell proliferationin vitro and tumor progression in mouse models. Such "two-in-one"antibodies challenge the monoclonal antibody paradigm of onebinding site, one antigen. They could also provide new opportunitiesfor antibody-based therapy.
1 Department of Protein Engineering, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA. 2 Department of Antibody Engineering, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA. 3 Department of Translational Oncology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA. 4 Department of Assay and Automation Technology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA. 5 Department of Pathology, Genentech, 1 DNA Way, South San Francisco, CA 94080, USA.
* To whom correspondence should be addressed. E-mail: gml{at}gene.com
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