Fc fusion
    5.
    发明申请
    Fc fusion 审中-公开
    Fc融合

    公开(公告)号:US20060083747A1

    公开(公告)日:2006-04-20

    申请号:US11166496

    申请日:2005-06-24

    摘要: The present invention relates to a simple method for generating antibody-based structures suitable for in vivo use. In particular, the invention relates to a method for the generation of antibody-based structures suitable for in vivo use comprising the steps of: (a) selecting an antibody single variable domain having an epitope binding specificity; and (b) attaching the single domain of step (a) to an effector group. Uses of molecules generated using the method of the Invention are also described.

    摘要翻译: 本发明涉及一种生成适用于体内使用的基于抗体的结构的简单方法。 特别地,本发明涉及一种生成适合于体内应用的基于抗体的结构的方法,包括以下步骤:(a)选择具有表位结合特异性的抗体单可变结构域; 和(b)将步骤(a)的单一结构域连接到效应子组。 还描述了使用本发明的方法生成的分子的用途。

    Retargeting
    6.
    发明申请
    Retargeting 审中-公开
    重新定位

    公开(公告)号:US20060280734A1

    公开(公告)日:2006-12-14

    申请号:US11165672

    申请日:2005-06-24

    CPC分类号: C07K16/005

    摘要: The present invention relates to a method for the generation of immunoglobulin molecules of predetermined specificity. In particular, the invention relates to a method for the retargeting of the epitope binding specificity of one or more antibodies using single variable domains which exhibit a dominant epitope binding specificity.

    摘要翻译: 本发明涉及产生具有预定特异性的免疫球蛋白分子的方法。 特别地,本发明涉及使用显示优势表位结合特异性的单个可变结构域重定向一种或多种抗体的表位结合特异性的方法。

    Method to screen phage display libraries with different ligands
    7.
    发明授权
    Method to screen phage display libraries with different ligands 有权
    用不同配体筛选噬菌体展示文库的方法

    公开(公告)号:US06846634B1

    公开(公告)日:2005-01-25

    申请号:US09511939

    申请日:2000-02-24

    摘要: The invention provides a method for selecting, from a repertoire of polypeptides, a population of functional polypeptides which bind a target ligand in a first binding site and a generic ligand in a second binding site, which generic ligand is capable of binding functional members of the repertoire regardless of target ligand specificity, comprising the steps of: a) contacting the repertoire with the generic ligand and selecting functional polypeptides bound thereto; and b) contacting the selected functional polypeptides with the target ligand and selecting a population of polypeptides which bind to the target ligand. The invention accordingly provides a method by which a polypeptide repertoire is preselected, according to functionality as determined by the ability to bind the generic ligand, and the subset of polypeptides obtained as a result of such preselection is then employed for further selection according to the ability to bind the target ligand.

    摘要翻译: 本发明提供了从多肽的所有组成部分中选择结合第一结合位点中的靶配体和第二结合位点中的通用配体的功能性多肽群体的方法,该通用配体能够结合 包括以下步骤:a)使所述谱系与通用配体接触并选择与其结合的功能性多肽; 和b)使所选择的功能性多肽与靶配体接触并选择结合靶配体的多肽群体。 因此,本发明提供了根据通过结合通用配体的能力所确定的官能度来预先选择多肽集合的方法,然后根据能力进一步选择作为这种预选的结果的多肽获得的子集 以结合靶配体。

    Methods for selecting functional polypeptides
    8.
    发明授权
    Methods for selecting functional polypeptides 失效
    选择功能性多肽的方法

    公开(公告)号:US06696245B2

    公开(公告)日:2004-02-24

    申请号:US09192854

    申请日:1998-11-17

    IPC分类号: C12Q170

    摘要: The invention provides a method for selecting, from a repertoire of polypeptides, a population of functional polypeptides which bind a target ligand in a first binding site and a generic ligand in a second binding site, which generic ligand is capable of binding functional members of the repertoire regardless of target ligand specificity, comprising the steps of: a) contacting the repertoire with the generic ligand and selecting functional polypeptides bound thereto; and b) contacting the selected functional polypeptides with the target ligand and selecting a population of polypeptides which bind to the target ligand. The invention accordingly provides a method by which a polypeptide repertoire is preselected, according to functionality as determined by the ability to bind the generic ligand, and the subset of polypeptides obtained as a result of such preselection is then employed for further selection according to the ability to bind the target ligand.

    摘要翻译: 本发明提供了从多肽的所有组成部分中选择结合第一结合位点中的靶配体和第二结合位点中的通用配体的功能性多肽群体的方法,该通用配体能够结合 包括以下步骤:a)使所述谱系与通用配体接触并选择与其结合的功能性多肽; 和b)使所选择的功能性多肽与靶配体接触并选择结合靶配体的多肽群体。 因此,本发明提供了根据通过结合通用配体的能力确定的官能度来预先选择多肽集合的方法,然后根据该预选的能力进一步选择作为这种预选结果的多肽获得的子集 以结合靶配体。