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The structural basis for the function of two anti-VEGF receptor 2 antibodies.
Franklin, Matthew C; Navarro, Elizabeth C; Wang, Yujie; Patel, Sheetal; Singh, Pinki; Zhang, Yi; Persaud, Kris; Bari, Amtul; Griffith, Heather; Shen, Leyi; Balderes, Paul; Kussie, Paul.
Affiliation
  • Franklin MC; Department of Immunology, ImClone Systems, New York, NY 10014, USA. mfranklin@nysbc.org
Structure ; 19(8): 1097-107, 2011 Aug 10.
Article in En | MEDLINE | ID: mdl-21827946
ABSTRACT
The anti-VEGF receptor 2 antibody IMC-1121B is a promising antiangiogenic drug being tested for treatment of breast and gastric cancer. We have determined the structure of the 1121B Fab fragment in complex with domain 3 of VEGFR2, as well as the structure of a different neutralizing anti-VEGFR2 antibody, 6.64, also in complex with VEGFR2 domain 3. The two Fab fragments bind at opposite ends of VEGFR2 domain 3; 1121B directly blocks VEGF binding, whereas 6.64 may prevent receptor dimerization by perturbing the domain 3domain 4 interface. Mutagenesis reveals that residues essential for VEGF, 1121B, and 6.64 binding are nonoverlapping among the three contact patches.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Angiogenesis Inhibitors / Vascular Endothelial Growth Factor Receptor-2 / Antibodies, Monoclonal Type of study: Prognostic_studies Language: En Journal: Structure Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / BIOTECNOLOGIA Year: 2011 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Angiogenesis Inhibitors / Vascular Endothelial Growth Factor Receptor-2 / Antibodies, Monoclonal Type of study: Prognostic_studies Language: En Journal: Structure Journal subject: BIOLOGIA MOLECULAR / BIOQUIMICA / BIOTECNOLOGIA Year: 2011 Document type: Article Affiliation country:
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