Sequence-directed DNA-binding molecules compositions and methods
    1.
    发明授权
    Sequence-directed DNA-binding molecules compositions and methods 失效
    序列指导的DNA结合分子的组成和方法

    公开(公告)号:US06869765B2

    公开(公告)日:2005-03-22

    申请号:US09993346

    申请日:2001-11-13

    摘要: The present invention defines a DNA: protein-binding assay useful for screening libraries of synthetic or biological compounds for their ability to bind DNA test sequences. The assay is versatile in that any number of test sequences can be tested by placing the test sequence adjacent to a defined protein binding screening sequence. Binding of molecules to these test sequence changes the binding characteristics of the protein molecule to its cognate binding sequence. When such a molecule binds the test sequence the equilibrium of the DNA:protein complexes is disturbed, generating changes in the concentration of free DNA probe. Numerous exemplary target test sequences (SEQ ID NO:1 to SEQ ID NO:600) are set forth. The assay of the present invention is also useful to characterize the preferred binding sequences of any selected DNA-binding molecule.

    摘要翻译: 本发明定义了一种DNA:蛋白结合测定法,用于筛选合成或生物化合物文库结合DNA测试序列的能力。 该测定法是通用的,因为可以通过将测试序列置于与定义的蛋白质结合筛选序列相邻的位置来测试任何数量的测试序列。 分子与这些测试序列的结合改变了蛋白质分子与其同源结合序列的结合特征。 当这样的分子结合测试序列时,DNA:蛋白复合物的平衡受到干扰,产生游离DNA探针浓度的变化。 阐述了许多示例性目标测试序列(SEQ ID NO:1至SEQ ID NO:600)。 本发明的测定也可用于表征任何所选DNA结合分子的优选结合序列。

    Method of determining DNA sequence preference of a DNA-binding molecule
    2.
    发明授权
    Method of determining DNA sequence preference of a DNA-binding molecule 失效
    确定DNA结合分子DNA序列偏好的方法

    公开(公告)号:US5869241A

    公开(公告)日:1999-02-09

    申请号:US475228

    申请日:1995-06-07

    摘要: The present invention defines a DNA:protein-binding assay useful for screening libraries of synthetic or biological compounds for their ability to bind DNA test sequences. The assay is versatile in that any number of test sequences can be tested by placing the test sequence adjacent to a defined protein binding screening sequence. Binding of molecules to these test sequence changes the binding characteristics of the protein molecule to its cognate binding sequence. When such a molecule binds the test sequence the equilibrium of the DNA:protein complexes is disturbed, generating changes in the concentration of free DNA probe. Numerous exemplary target test sequences (SEQ ID NO:1 to SEQ ID NO:600) are set forth. The assay of the present invention is also useful to characterize the preferred binding sequences of any selected DNA-binding molecule.

    摘要翻译: 本发明定义了一种DNA:蛋白结合测定法,用于筛选合成或生物化合物文库结合DNA测试序列的能力。 该测定法是通用的,因为可以通过将测试序列置于与定义的蛋白质结合筛选序列相邻的位置来测试任何数量的测试序列。 分子与这些测试序列的结合改变了蛋白质分子与其同源结合序列的结合特征。 当这样的分子结合测试序列时,DNA:蛋白复合物的平衡受到干扰,产生游离DNA探针浓度的变化。 阐述了许多示例性目标测试序列(SEQ ID NO:1至SEQ ID NO:600)。 本发明的测定也可用于表征任何所选DNA结合分子的优选结合序列。

    Sequence-directed DNA-binding molecules compositions and methods
    3.
    发明授权
    Sequence-directed DNA-binding molecules compositions and methods 失效
    序列指导的DNA结合分子的组成和方法

    公开(公告)号:US5578444A

    公开(公告)日:1996-11-26

    申请号:US171389

    申请日:1993-12-20

    摘要: The present invention defines a DNA:protein-binding assay useful for screening libraries of synthetic or biological compounds for their ability to bind DNA test sequences. The assay is versatile in that any number of test sequences can be tested by placing the test sequence adjacent to a defined protein binding screening sequence. Binding of molecules to these test sequence changes the binding characteristics of the protein molecule to its cognate binding sequence. When such a molecule binds the test sequence the equilibrium of the DNA:protein complexes is disturbed, generating changes in the concentration of free DNA probe. Numerous exemplary target test sequences (SEQ ID NO:1 to SEQ ID NO:600) are set forth. The assay of the present invention is also useful to characterize the preferred binding sequences of any selected DNA-binding molecule.

    摘要翻译: 本发明定义了一种DNA:蛋白结合测定法,用于筛选合成或生物化合物文库结合DNA测试序列的能力。 该测定法是通用的,因为可以通过将测试序列置于与定义的蛋白质结合筛选序列相邻的位置来测试任何数量的测试序列。 分子与这些测试序列的结合改变了蛋白质分子与其同源结合序列的结合特征。 当这样的分子结合测试序列时,DNA:蛋白复合物的平衡受到干扰,产生游离DNA探针浓度的变化。 阐述了许多示例性目标测试序列(SEQ ID NO:1至SEQ ID NO:600)。 本发明的测定也可用于表征任何所选DNA结合分子的优选结合序列。

    Sequence-directed DNA binding molecules compositions and methods
    4.
    发明授权
    Sequence-directed DNA binding molecules compositions and methods 失效
    序列指导的DNA结合分子的组成和方法

    公开(公告)号:US6010849A

    公开(公告)日:2000-01-04

    申请号:US482080

    申请日:1995-06-07

    摘要: The present invention defines a DNA:protein-binding assay useful for screening libraries of synthetic or biological compounds for their ability to bind DNA test sequences. The assay is versatile in that any number of test sequences can be tested by placing the test sequence adjacent to a defined protein binding screening sequence. Binding of molecules to these test sequence changes the binding characteristics of the protein molecule to its cognate binding sequence. When such a molecule binds the test sequence the equilibrium of the DNA:protein complexes is disturbed, generating changes in the concentration of free DNA probe. Numerous exemplary target test sequences (SEQ ID NO:1 to SEQ ID NO:600) are set forth. The assay of the present invention is also useful to characterize the preferred binding sequences of any selected DNA-binding molecule.

    摘要翻译: 本发明定义了一种DNA:蛋白结合测定法,用于筛选合成或生物化合物文库结合DNA测试序列的能力。 该测定法是通用的,因为可以通过将测试序列置于与定义的蛋白质结合筛选序列相邻的位置来测试任何数量的测试序列。 分子与这些测试序列的结合改变了蛋白质分子与其同源结合序列的结合特征。 当这样的分子结合测试序列时,DNA:蛋白复合物的平衡受到干扰,产生游离DNA探针浓度的变化。 阐述了许多示例性目标测试序列(SEQ ID NO:1至SEQ ID NO:600)。 本发明的测定也可用于表征任何所选DNA结合分子的优选结合序列。

    Sequence directed DNA binding molecules compositions and methods
    5.
    发明授权
    Sequence directed DNA binding molecules compositions and methods 失效
    序列定向DNA结合分子的组成和方法

    公开(公告)号:US06384208B1

    公开(公告)日:2002-05-07

    申请号:US09354947

    申请日:1999-07-15

    IPC分类号: C07H2104

    摘要: The present invention defines a DNA: protein-binding assay useful for screening libraries of synthetic or biological compounds for their ability to bind DNA test sequences. The assay is versatile in that any number of test sequences can be tested by placing the test sequence adjacent to a defined protein binding screening sequence. Binding of molecules to these test sequence changes the binding characteristics of the protein molecule to its cognate binding sequence. When such a molecule binds the test sequence the equilibrium of the DNA:protein complexes is disturbed, generating changes in the concentration of free DNA probe. Numerous exemplary target test sequences (SEQ ID NO:1 to SEQ ID NO:600) are set forth. The assay of the present invention is also useful to characterize the preferred binding sequences of any selected DNA-binding molecule.

    摘要翻译: 本发明定义了一种DNA:蛋白结合测定法,用于筛选合成或生物化合物文库结合DNA测试序列的能力。 该测定法是通用的,因为可以通过将测试序列置于与定义的蛋白质结合筛选序列相邻的位置来测试任何数量的测试序列。 分子与这些测试序列的结合改变了蛋白质分子与其同源结合序列的结合特征。 当这样的分子结合测试序列时,DNA:蛋白复合物的平衡受到干扰,产生游离DNA探针浓度的变化。 阐述了许多示例性目标测试序列(SEQ ID NO:1至SEQ ID NO:600)。 本发明的测定也可用于表征任何所选DNA结合分子的优选结合序列。

    Screening assay for the detection of DNA-binding molecules
    6.
    发明授权
    Screening assay for the detection of DNA-binding molecules 失效
    检测DNA结合分子的筛选试验

    公开(公告)号:US5726014A

    公开(公告)日:1998-03-10

    申请号:US123936

    申请日:1993-09-17

    摘要: The present invention defines a DNA:protein-binding assay useful for screening libraries of synthetic or biological compounds for their ability to bind DNA test sequences. The assay is versatile in that any number of test sequences can be tested by placing the test sequence adjacent to a defined protein binding screening sequence. Binding of molecules to these test sequence changes the binding characteristics of the protein molecule to its cognate binding sequence. When such a molecule binds the test sequence the equilibrium of the DNA:protein complexes is disturbed, generating changes in the concentration of free DNA probe. Numerous exemplary target test sequences (SEQ ID NO:1 to SEQ ID NO:600) are set forth. The assay of the present invention is also useful to characterize the preferred binding sequences of any selected DNA-binding molecule.

    摘要翻译: 本发明定义了一种DNA:蛋白结合测定法,用于筛选合成或生物化合物文库结合DNA测试序列的能力。 该测定法是通用的,因为可以通过将测试序列置于与定义的蛋白质结合筛选序列相邻的位置来测试任何数量的测试序列。 分子与这些测试序列的结合改变了蛋白质分子与其同源结合序列的结合特征。 当这样的分子结合测试序列时,DNA:蛋白复合物的平衡受到干扰,产生游离DNA探针浓度的变化。 阐述了许多示例性目标测试序列(SEQ ID NO:1至SEQ ID NO:600)。 本发明的测定也可用于表征任何所选DNA结合分子的优选结合序列。