Sequence-directed DNA-binding molecules compositions and methods
    41.
    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

    Abstract: 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.

    Abstract translation: 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
    42.
    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

    Abstract: 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.

    Abstract translation: 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。

    Immuno-polymerase chain reaction system for antigen detection
    44.
    发明授权
    Immuno-polymerase chain reaction system for antigen detection 失效
    抗原检测免疫聚合酶链反应体系

    公开(公告)号:US5665539A

    公开(公告)日:1997-09-09

    申请号:US131301

    申请日:1993-10-04

    CPC classification number: C07K14/31 B82Y5/00 C07K14/36 A61K38/00

    Abstract: A novel system and method for sensitive antigen detection. The system utilizes immuno-polymerase chain reaction in which a specific biotinylated nucleic acid molecule is used as the marker. The biotinylated marker is attached to antigen-antibody complex through a streptavidin-protein A chimeric protein that possesses tight and specific binding affinity both for biotin and immunoglobulin G. A segment of the attached biotinylated marker is amplified by polymerase chain reactions with appropriate primers and the polymerase chain reaction products are detected by agarose gel electrophoresis. The method can detect any antigen and has a greater sensitivity than any existing antigen detection system.

    Abstract translation: 一种用于敏感抗原检测的新型系统和方法。 该系统利用免疫聚合酶链反应,其中使用特异性生物素化的核酸分子作为标记。 生物素标记通过链霉抗生物素蛋白 - 蛋白A嵌合蛋白连接到抗原 - 抗体复合物上,该嵌合蛋白对于生物素和免疫球蛋白G都具有紧密和特异性的结合亲和力。通过与适当引物的聚合酶链反应扩增连接的生物素标记的片段,并且 通过琼脂糖凝胶电泳检测聚合酶链反应产物。 该方法可以检测任何抗原并且比任何现有的抗原检测系统具有更高的灵敏度。

    Design and synthesis of bispecific DNA-antibody conjugates
    45.
    发明授权
    Design and synthesis of bispecific DNA-antibody conjugates 失效
    双特异性DNA抗体缀合物的设计与合成

    公开(公告)号:US5635602A

    公开(公告)日:1997-06-03

    申请号:US107186

    申请日:1993-08-13

    CPC classification number: C07K16/2812 C07K16/2809 C07K16/468

    Abstract: The invention relates to bis-protein-DNA conjugates. A protein having an antigen specific binding activity is covalently linked to each end of a derivatized DNA molecule. The bis-protein-DNA conjugates can be used for immunoassays and measuring distances between proteins at up to 3.4 .ANG. resolution. The invention also relates to methods of synthesizing these bis-protein-DNA conjugates. Synthesis of the conjugates entails derivatizing the 5' or 3' end of a DNA oligonucleotide and covalently linking that DNA to a protein. The DNA can be indirectly conjugated to an antibody or Fab' fragment, using a avidin/streptavidin-biotin linkage. The conjugates of the invention can be used in immunoassays and PCR assays.

    Abstract translation: 本发明涉及双蛋白-DNA缀合物。 具有抗原特异性结合活性的蛋白质与衍生的DNA分子的每个末端共价连接。 双蛋白-DNA缀合物可用于免疫测定,并以高达3.4 ANGSTROM分辨率测量蛋白质之间的距离。 本发明还涉及合成这些双蛋白-DNA缀合物的方法。 共轭物的合成需要衍生DNA寡核苷酸的5'或3'末端并共价连接该DNA与蛋白质。 可以使用抗生物素蛋白/链霉抗生物素蛋白 - 生物素连接,将DNA间接缀合至抗体或Fab'片段。 本发明的缀合物可用于免疫测定和PCR测定。

    DNA purification by triplex-affinity capture and affinity capture
electrophoresis
    48.
    发明授权
    DNA purification by triplex-affinity capture and affinity capture electrophoresis 失效
    通过三重亲和捕获和亲和捕获电泳进行DNA纯化

    公开(公告)号:US5482836A

    公开(公告)日:1996-01-09

    申请号:US4552

    申请日:1993-01-14

    CPC classification number: C12Q1/6839 C12N15/1003 C12N15/101 C12Q1/6806

    Abstract: The invention provides a method for purifying or isolating double stranded DNA intact using triple helix formation. The method includes the steps of complexing an oligonucleotide and double stranded DNA to generate a triple helix and immobilization of the triple helix on a solid phase by means of a molecular recognition system such as avidin/biotin. The purified DNA is then recovered intact by treating the solid phase with a reagent that breaks the bonds between the oligonucleotide and the intact double stranded DNA while not affecting the Watson-Crick base pairs of the double helix. The present invention also provides a method for purifying or isolating double stranded DNA intact by complexing the double stranded DNA with a specific binding partner and recovering the complex during electrophoresis by immobilizing it on a solid phase trap imbedded in an electrophoretic gel.

    Abstract translation: 本发明提供了使用三螺旋形成来纯化或分离完整的双链DNA的方法。 该方法包括以下步骤:使寡核苷酸和双链DNA复合以产生三螺旋,并通过分子识别系统如抗生物素蛋白/生物素将固定三固定在固相上。 然后通过用破坏寡核苷酸和完整双链DNA之间的键的试剂处理固相,同时不影响双螺旋的Watson-Crick碱基对,完整地回收纯化的DNA。 本发明还提供了通过使双链DNA与特异性结合配偶体络合来纯化或分离双链DNA的方法,并通过将其固定在嵌入电泳凝胶中的固相捕集器上,在电泳过程中回收该配合物。

    Screening assay for the detection of DNA-binding molecules
    49.
    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:US5306619A

    公开(公告)日:1994-04-26

    申请号:US81070

    申请日:1993-06-22

    Abstract: 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. Also described herein is a method to capture DNA that has been released from the DNA:protein complex.

    Abstract translation: 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。 本文还描述了捕获已经从DNA:蛋白质复合物释放的DNA的方法。

    METHODS AND COMPOSITIONS FOR THE ANALYSIS OF BIOLOGICAL MOLECULES
    50.
    发明申请
    METHODS AND COMPOSITIONS FOR THE ANALYSIS OF BIOLOGICAL MOLECULES 有权
    生物分子分析的方法和组合

    公开(公告)号:US20110124518A1

    公开(公告)日:2011-05-26

    申请号:US12863169

    申请日:2009-01-16

    Abstract: Provided herein are compositions and methods for analysis of nucleic acids, including, methods and compositions for genotyping, haplotyping, sequencing and performing other genetic and epigenetic analyses on nucleic acids, for example. In some embodiments, methods and compositions suitable for whole-genome sequencing on single molecules of nucleic acid are provided. In some embodiments, analysis of single molecules of nucleic acid are performed in conjunction with nanopores and/or nanopore devices.

    Abstract translation: 本文提供了用于分析核酸的组合物和方法,包括用于例如基因分型,单倍型,测序和对核酸进行其它遗传和表观遗传学分析的方法和组合物。 在一些实施方案中,提供适用于单分子核酸上的全基因组测序的方法和组合物。 在一些实施方案中,结合纳米孔和/或纳米孔装置进行单分子核酸的分析。

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