期刊论文详细信息
FEBS Letters
Formation of a high affinity heregulin binding site using the soluble extracellular domains of ErbB2 with ErbB3 or ErbB4
Pisacane, Paul I1  Vandlen, Richard L1  Sliwkowski, Mark X1  Fitzpatrick, V.Danial1 
[1] Genentech, Inc., Department of Molecular Oncology, 1 DNA Way, Mail Stop 63, South San Francisco, CA 94080, USA
关键词: Affinity modulation;    ErbB receptor;    HER2-neu;    Neuregulin;    Transactivation;    EGFR;    epidermal growth factor receptor;    EGF;    epidermal growth factor;    HRG;    heregulin;    also called neu differentiation factor or neuregulin;    ECD;    extracellular domain;    ErbB2-IgG;    homodimeric fusion protein between the ECD of ErbB2 with the human IgG heavy chain (other homodimeric constructs are ErbB3-IgG and ErbB4-IgG);    ErbB2/3-IgG;    heterodimeric fusion protein between the ECD of ErbB2 and ErbB3 with the human IgG heavy chain (other heterodimeric constructs are ErbB2/4-IgG and ErbB3/4-IgG);   
DOI  :  10.1016/S0014-5793(98)00737-6
学科分类:生物化学/生物物理
来源: John Wiley & Sons Ltd.
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【 摘 要 】

ErbB2 functions as a shared signal transducing component for other ErbB receptor family members. Two of these receptors, ErbB3 and ErbB4, bind the heregulin (HRG) or neuregulin family of polypeptide growth factors. Cells expressing ErbB3 alone display a single class of low affinity HRG binding sites, whereas both high and low affinity binding sites can be measured on cells that co-express both ErbB3 and ErbB2. To assess the interaction of the extracellular domains of ErbB receptors, a series of soluble homodimeric and heterodimeric IgG fusion proteins were constructed. Heregulin binding analysis revealed that a heterodimer composed of either ErbB3 or ErbB4 with ErbB2 is sufficient for the formation of a high affinity binding state. In contrast, heterodimeric ErbB3/4-IgG, as well as homodimeric ErbB3-IgG or ErbB4-IgG, contained only low affinity HRG binding sites. Further evidence for the unique specificity of ErbB2 in generating this high affinity binding site was determined by inhibiting HRG binding with an ErbB2 monoclonal antibody.

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