Screening assay for the detection of DNA-binding molecules
    1.
    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。

    Sequence-directed DNA binding molecules compositions and methods
    2.
    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
    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: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
    4.
    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
    5.
    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
    6.
    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。

    Method of constructing sequence-specific DNA-binding molecules
    8.
    发明授权
    Method of constructing sequence-specific DNA-binding molecules 失效
    构建序列特异性DNA结合分子的方法

    公开(公告)号:US5716780A

    公开(公告)日:1998-02-10

    申请号:US484499

    申请日:1995-06-07

    摘要: The present invention defines an assay useful for screening libraries of synthetic or biological compounds for their ability to bind specific DNA test sequences. The assay is also useful for determining the sequence specificity and relative DNA-binding affinity of DNA-binding molecules for any particular DNA sequence. Also described herein are potential applications of the assay, including: 1) the detection of lead compounds or new drugs via the mass screening of libraries of synthetic or biological compounds (i.e., fermentation broths); 2) the design of sequence-specific DNA-binding drugs comprised of homo- or hetero-meric subunits of molecules for which the sequence specificity was determined using the assay; and 3) the use of molecules for which sequence specificity was determined using the assay as covalently attached moieties to aid in the binding of nucleic acid or other macromolecular polymers to nucleic acid sequences.

    摘要翻译: 本发明定义了一种用于筛选合成或生物化合物文库以测定其结合特异性DNA测试序列的能力的测定法。 该测定还可用于确定DNA结合分子对于任何特定DNA序列的序列特异性和相对DNA结合亲和力。 本文还描述了测定的潜在应用,包括:1)通过大量筛选合成或生物化合物(即发酵液)文库来检测铅化合物或新药物; 2)由使用该测定法确定序列特异性的分子的同源或异源亚基组成的序列特异性DNA结合药物的设计; 和3)使用通过测定作为共价连接的部分确定序列特异性的分子,以有助于核酸或其它大分子聚合物与核酸序列的结合。

    Sequence-directed DNA-binding molecules compositions and methods
    9.
    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:US5738990A

    公开(公告)日:1998-04-14

    申请号:US475221

    申请日:1995-06-07

    摘要: The present invention defines an assay useful for screening libraries of synthetic or biological compounds for their ability to bind specific DNA test sequences. The assay is also useful for determining the sequence specificity and relative DNA-binding affinity of DNA-binding molecules for any particular DNA sequence. Also described herein are potential applications of the assay, including: 1) the detection of lead compounds or new drugs via the mass screening of libraries of synthetic or biological compounds (i.e., fermentation broths); 2) the design of sequence-specific DNA-binding drugs comprised of homo- or hetero-meric subunits of molecules for which the sequence specificity was determined using the assay; and 3) the use of molecules for which sequence specificity was determined using the assay as covalently attached moieties to aid in the binding of nucleic acid or other macromolecular polymers to nucleic acid sequences.

    摘要翻译: 本发明定义了一种用于筛选合成或生物化合物文库以测定其结合特异性DNA测试序列的能力的测定法。 该测定还可用于确定DNA结合分子对于任何特定DNA序列的序列特异性和相对DNA结合亲和力。 本文还描述了测定的潜在应用,包括:1)通过大量筛选合成或生物化合物(即发酵液)文库来检测铅化合物或新药物; 2)由使用该测定法确定序列特异性的分子的同源或异源亚基组成的序列特异性DNA结合药物的设计; 和3)使用通过测定作为共价连接的部分确定序列特异性的分子,以有助于核酸或其它大分子聚合物与核酸序列的结合。

    Method of ordering sequence binding preferences of a DNA-binding molecule
    10.
    发明授权
    Method of ordering sequence binding preferences of a DNA-binding molecule 失效
    排序DNA结合分子的序列结合偏好的方法

    公开(公告)号:US5693463A

    公开(公告)日:1997-12-02

    申请号:US996783

    申请日:1992-12-23

    摘要: The present invention defines an assay useful for screening libraries of synthetic or biological compounds for their ability to bind specific DNA test sequences. The assay is also useful for determining the sequence specificity and relative DNA-binding affinity of DNA-binding molecules for any particular DNA sequence. Also described herein are potential applications of the assay, including: 1) the detection of lead compounds or new drugs via the mass screening of libraries of synthetic or biological compounds (i.e., fermentation broths); 2) the design of sequence-specific DNA-binding drugs comprised of homo- or hetero-meric subunits of molecules for which the sequence specificity was determined using the assay; and 3) the use of molecules for which sequence specificity was determined using the assay as covalently attached moieties to aid in the binding of nucleic acid or other macromolecular polymers to nucleic acid sequences.

    摘要翻译: 本发明定义了一种用于筛选合成或生物化合物文库以测定其结合特异性DNA测试序列的能力的测定法。 该测定还可用于确定DNA结合分子对于任何特定DNA序列的序列特异性和相对DNA结合亲和力。 本文还描述了测定的潜在应用,包括:1)通过大量筛选合成或生物化合物(即发酵液)文库来检测铅化合物或新药物; 2)由使用该测定法确定序列特异性的分子的同源或异源亚基组成的序列特异性DNA结合药物的设计; 和3)使用通过测定作为共价连接的部分确定序列特异性的分子,以有助于核酸或其它大分子聚合物与核酸序列的结合。