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    • 1. 发明申请
    • Membrane-Translocating Peptides
    • 膜 - 位移肽
    • US20080287311A1
    • 2008-11-20
    • US11996496
    • 2006-07-24
    • David CoomberKevin FitzgeraldDuncan McGregorChris UllmanTomas Leanderson
    • David CoomberKevin FitzgeraldDuncan McGregorChris UllmanTomas Leanderson
    • C40B30/04C07K14/00C07H21/00C12N5/06
    • C12N15/1075
    • A method is provided for selecting membrane-translocating peptides (MTPs) from a peptide display library that are capable of crossing or penetrating a lipid membrane. A plurality of nucleic acid constructs that encode displayed peptides are expressed, resulting in the formation of a plurality of nucleic acid-peptide complexes, each complex comprising at least one displayed peptide associated with the corresponding nucleic acid construct encoding the displayed peptide; the complexes are exposed to a population of membrane-encapsulated compartments, allowing a translocating reaction to occur; complexes that remain unassociated with the membrane are removed; optionally complexes that are associated with the membrane are removed; and internalised nucleic acid-peptide complexes are recovered. The membrane-encapsulated compartments may be artificial vesicles such as liposomes, or populations of one or more cell types.
    • 提供了从能够穿透或穿透脂质膜的肽展示文库中选择膜转位肽(MTP)的方法。 表达编码显示的肽的多个核酸构建体,导致形成多个核酸 - 肽复合物,每个复合物包含与编码所显示肽的相应核酸构建体相关联的至少一个显示的肽; 复合物暴露于膜包封的隔室群,允许发生易位反应; 与膜保持不相关的复合物被去除; 去除与膜相关的任选复合物; 并回收内化的核酸 - 肽复合物。 膜包封的隔室可以是人造囊泡,例如脂质体或一种或多种细胞类型的群体。
    • 2. 发明授权
    • Membrane-translocating peptides
    • 膜易位肽
    • US08557744B2
    • 2013-10-15
    • US11996496
    • 2006-07-24
    • David CoomberKevin FitzgeraldDuncan McGregorChris UllmanTomas Leanderson
    • David CoomberKevin FitzgeraldDuncan McGregorChris UllmanTomas Leanderson
    • C40B30/04C12Q1/70
    • C12N15/1075
    • A method is selects membrane-translocating peptides (MTPs) from a peptide display library that are capable of crossing or penetrating a lipid membrane. A plurality of nucleic acid constructs that encode displayed peptides are expressed, resulting in the formation of a plurality of nucleic acid-peptide complexes, each complex comprising at least one displayed peptide associated with the corresponding nucleic acid construct encoding the displayed peptide; the complexes are exposed to a population of membrane-encapsulated compartments, allowing a translocating reaction to occur; complexes that remain unassociated with the membrane are removed; optionally complexes that are associated with the membrane are removed; and internalized nucleic acid-peptide complexes are recovered. The membrane-encapsulated compartments may be artificial vesicles such as liposomes, or populations of one or more cell types.
    • 一种方法是从能够穿透或穿透脂质膜的肽展示文库中选择膜 - 位移肽(MTP)。 表达编码显示的肽的多个核酸构建体,导致形成多个核酸 - 肽复合物,每个复合物包含与编码所显示肽的相应核酸构建体相关联的至少一个显示的肽; 复合物暴露于膜包封的隔室群,允许发生易位反应; 与膜保持不相关的复合物被去除; 去除与膜相关的任选复合物; 并回收内化的核酸 - 肽复合物。 膜包封的隔室可以是人造囊泡,例如脂质体或一种或多种细胞类型的群体。
    • 8. 发明授权
    • Chimeric binding peptide library screening method
    • 嵌合结合肽库筛选方法
    • US07312074B1
    • 2007-12-25
    • US09486882
    • 1998-09-02
    • Duncan McGregor
    • Duncan McGregor
    • C12Q1/68C12N15/00
    • C07K14/70567C07K2319/00C12N15/1075
    • There is described a method of isolating nucleotide sequences encoding target peptides from DNA libraries using DNA binding proteins to link the peptide to the sequence which encodes it. DNA libraries are prepared from cells encoding the protein of interest, or from synthetic DNA, and inserted into, or adjacent to, a DNA binding protein in an expression vector to create a chimeric fusion protein. Incorporation of the vector DNA into a carrier package, during expression of the chimeric fusion protein, results in the production of a peptide display carrier package (PDCP) displaying the DNA-bound fusion protein on the external surface of the carrier package. Employment of affinity purification techniques results in the PDCP particles containing sequences encoding the desired peptide to be selected and the desired nucleotide sequences obtained therefrom.
    • 描述了使用DNA结合蛋白从DNA文库分离编码靶肽的核苷酸序列以将肽连接到编码它的序列的方法。 从编码目标蛋白的细胞或合成的DNA制备DNA文库,并将其插入到表达载体中的DNA结合蛋白中或与DNA结合蛋白相邻,以产生嵌合融合蛋白。 在嵌合融合蛋白的表达期间将载体DNA并入载体包中导致在载体包装的外表面上显示DNA结合融合蛋白的肽显示载体包装(PDCP)的制备。 使用亲和纯化技术导致含有编码要选择的所需肽的序列的PDCP颗粒和由其获得的所需核苷酸序列。
    • 10. 发明授权
    • Chimeric binding peptide library screening method
    • 嵌合结合肽库筛选方法
    • US08735146B2
    • 2014-05-27
    • US11985355
    • 2007-11-13
    • Duncan McGregor
    • Duncan McGregor
    • C12N15/00C12Q1/68
    • C07K14/70567C07K2319/00C12N15/1075
    • There is described a method of isolating nucleotide sequences encoding target peptides from DNA libraries using DNA binding proteins to link the peptide to the sequence which encodes it. DNA libraries are prepared from cells encoding the protein of interest, or from synthetic DNA, and inserted into, or adjacent to, a DNA binding protein in an expression vector to create a chimeric fusion protein. Incorporation of the vector DNA into a carrier package, during expression of the chimeric fusion protein, results in the production of a peptide display carrier package (PDCP) displaying the DNA-bound fusion protein on the external surface of the carrier package. Employment of affinity purification techniques results in the PDCP particles containing sequences encoding the desired peptide to be selected and the desired nucleotide sequences obtained therefrom.
    • 描述了使用DNA结合蛋白从DNA文库分离编码靶肽的核苷酸序列以将肽连接到编码它的序列的方法。 从编码目标蛋白的细胞或合成的DNA制备DNA文库,并将其插入到表达载体中的DNA结合蛋白中或与DNA结合蛋白相邻,以产生嵌合融合蛋白。 在嵌合融合蛋白的表达期间将载体DNA并入载体包中导致在载体包装的外表面上显示DNA结合融合蛋白的肽显示载体包装(PDCP)的制备。 使用亲和纯化技术导致含有编码要选择的所需肽的序列的PDCP颗粒和由其获得的所需核苷酸序列。