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公开(公告)号:US5422104A
公开(公告)日:1995-06-06
申请号:US794400
申请日:1991-11-20
申请人: Walter Fiers , Jan Tavernier , Xaveer Van Ostade
发明人: Walter Fiers , Jan Tavernier , Xaveer Van Ostade
IPC分类号: A61K38/00 , A61P35/00 , C07K14/52 , C07K14/525 , C12N1/21 , C12N15/09 , C12N15/28 , C12P21/02 , C12R1/19 , A61K45/05 , C12P21/06
CPC分类号: C07K14/525 , A61K38/00
摘要: It is an object of this invention to provide a human Tumor Necrosis Factor mutein or a pharmaceutically acceptable salt thereof characterized in that the TNF sequence is changed by a deletion, insertion, substitution or combinations thereof, of one or more amino acids so that the mutein shows a significant difference between its binding affinity to the human p75-Tumor-Necrosis-Factor-Receptor and to the human p55-Tumor-Necrosis-Factor-Receptor. The invention also includes DNA sequences coding for such muteins, vectors comprising such DNA sequences, host cells transformed with such vectors and a process for the production of such muteins employing such transformed host cells and pharmaceutical compositions containing such muteins and their use for the treatment of illnesses, for example cancer.
摘要翻译: 本发明的目的是提供一种人肿瘤坏死因子突变蛋白或其药学上可接受的盐,其特征在于通过其一个或多个氨基酸的缺失,插入,取代或组合改变TNF序列,使得突变蛋白 显示其与人p75-肿瘤坏死因子受体和人p55-肿瘤坏死因子受体的结合亲和力之间的显着差异。 本发明还包括编码这种突变蛋白的DNA序列,包含这种DNA序列的载体,用这种载体转化的宿主细胞和使用这种转化的宿主细胞产生这种突变蛋白的方法和含有这种突变蛋白的药物组合物及其用于治疗 疾病,例如癌症。
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公开(公告)号:US20100173408A1
公开(公告)日:2010-07-08
申请号:US12653484
申请日:2009-12-14
IPC分类号: C07K14/705 , C12N5/071 , C12N1/14 , C12N5/04
CPC分类号: C12N15/1055 , C07K14/71 , C07K14/715 , C07K2319/00 , C07K2319/02 , C07K2319/20 , C07K2319/70 , C07K2319/90 , C12N2799/027 , C12N2799/06
摘要: Described is a recombinant receptor comprising an extracellular ligand-binding domain and a cytoplasmic domain that comprises a heterologous bait polypeptide. The recombinant receptor is activated by binding of a ligand to the ligand-binding domain and by binding of a prey polypeptide to the heterologous bait peptide. The invention also discloses a method for detecting compound-compound binding using the recombinant receptor.
摘要翻译: 描述了包含细胞外配体结合结构域和包含异源诱饵多肽的细胞质结构域的重组受体。 通过将配体结合到配体结合结构域并通过将猎物多肽与异源诱饵肽的结合来激活重组受体。 本发明还公开了使用重组受体检测化合物 - 化合物结合的方法。
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公开(公告)号:US5652353A
公开(公告)日:1997-07-29
申请号:US397470
申请日:1995-03-01
申请人: Walter Fiers , Jan Tavernier , Xaveer Van Ostade
发明人: Walter Fiers , Jan Tavernier , Xaveer Van Ostade
IPC分类号: A61K38/00 , A61P35/00 , C07K14/52 , C07K14/525 , C12N1/21 , C12N15/09 , C12N15/28 , C12P21/02 , C12R1/19
CPC分类号: C07K14/525 , A61K38/00
摘要: It is an object of this invention to provide a human Tumor Necrosis Factor mutein or a pharmaceutically acceptable salt thereof characterized in that the TNF sequence is changed by a deletion, insertion, substitution or combinations thereof, of one or more amino acids so that the mutein shows a significant difference between its binding affinity to the human p75-Tumor-Necrosis-Factor-Receptor and to the human p55-Tumor-Necrosis-Factor-Receptor. The invention also includes DNA sequences coding for such muteins, vectors comprising such DNA sequences, host cells transformed with such vectors and a process for the production of such muteins employing such transformed host cells and pharmaceutical compositions containing such muteins and their use for the treatment of illnesses, for example cancer.
摘要翻译: 本发明的目的是提供一种人肿瘤坏死因子突变蛋白或其药学上可接受的盐,其特征在于通过其一个或多个氨基酸的缺失,插入,取代或组合改变TNF序列,使得突变蛋白 显示其与人p75-肿瘤坏死因子受体和人p55-肿瘤坏死因子受体的结合亲和力之间的显着差异。 本发明还包括编码这种突变蛋白的DNA序列,包含这种DNA序列的载体,用这种载体转化的宿主细胞和使用这种转化的宿主细胞产生这种突变蛋白的方法和含有这种突变蛋白的药物组合物及其用于治疗 疾病,例如癌症。
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公开(公告)号:US08003757B2
公开(公告)日:2011-08-23
申请号:US12653484
申请日:2009-12-14
IPC分类号: C07K19/00 , C12N5/10 , C12N1/15 , G01N33/566
CPC分类号: C12N15/1055 , C07K14/71 , C07K14/715 , C07K2319/00 , C07K2319/02 , C07K2319/20 , C07K2319/70 , C07K2319/90 , C12N2799/027 , C12N2799/06
摘要: Described is a recombinant receptor comprising an extracellular ligand-binding domain and a cytoplasmic domain that comprises a heterologous bait polypeptide. The recombinant receptor is activated by binding of a ligand to the ligand-binding domain and by binding of a prey polypeptide to the heterologous bait peptide. The invention also discloses a method for detecting compound-compound binding using the recombinant receptor.
摘要翻译: 描述了包含细胞外配体结合结构域和包含异源诱饵多肽的细胞质结构域的重组受体。 通过将配体结合到配体结合结构域并通过将猎物多肽与异源诱饵肽的结合来激活重组受体。 本发明还公开了使用重组受体检测化合物 - 化合物结合的方法。
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公开(公告)号:US07855270B2
公开(公告)日:2010-12-21
申请号:US10303157
申请日:2002-11-22
IPC分类号: C07K19/00 , C12N5/10 , C12N1/15 , G01N33/566
CPC分类号: C12N15/1055 , C07K14/71 , C07K14/715 , C07K2319/00 , C07K2319/02 , C07K2319/20 , C07K2319/70 , C07K2319/90 , C12N2799/027 , C12N2799/06
摘要: The present invention discloses a recombinant receptor comprising an extracellular ligand-binding domain and a cytoplasmic domain that comprises a heterologous bait polypeptide. The recombinant receptor is activated by binding of a ligand to the ligand binding domain and by binding of a prey polypeptide to the heterologous bait peptide. The present invention also discloses a method for detecting compound-compound binding using the recombinant receptor.
摘要翻译: 本发明公开了包含细胞外配体结合结构域和包含异源诱饵多肽的细胞质结构域的重组受体。 重组受体通过将配体结合到配体结合结构域并通过将猎物多肽与异源诱饵肽结合来活化。 本发明还公开了使用重组受体检测化合物 - 化合物结合的方法。
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