METHOD FOR IDENTIFYING POLYUBIQUITINATED SUBSTRATE
    1.
    发明公开
    METHOD FOR IDENTIFYING POLYUBIQUITINATED SUBSTRATE 有权
    VERFAHREN ZUR IDENTIFIKATION POLYUBIQUITINIERTER SUBSTRATE

    公开(公告)号:EP3070176A4

    公开(公告)日:2017-05-03

    申请号:EP14863005

    申请日:2014-11-13

    IPC分类号: C12Q1/527 C12N15/09 C12Q1/37

    摘要: An object of the present invention is to provide a method for efficiently identifying a polyubiquitinated substrate which is generally not easily identified. The method for identifying a polyubiquitinated substrate includes (1) a step of expressing a trypsin-resistant polyubiquitin chain-binding protein and a ubiquitin ligase in a cell, (2) a step of isolating a complex that contains the trypsin-resistant polyubiquitin chain-binding protein from the cell having undergone the step (1), (3) a step of subjecting the complex isolated by the step (2) to trypsin digestion, and (4) a step of identifying a peptide that has a ubiquitination site from a digested material obtained by the step (3).

    摘要翻译: 本发明的一个目的是提供一种用于有效鉴定通常不易鉴定的多聚遍在蛋白化底物的方法。 鉴定多聚泛素化底物的方法包括:(1)在细胞中表达胰蛋白酶抗性多聚遍在蛋白链结合蛋白和泛蛋白连接酶的步骤;(2)分离含有胰蛋白酶抗性多聚遍在蛋白链结合蛋白的复合物的步骤; (3)使步骤(2)分离的复合物进行胰蛋白酶消化的步骤,和(4)从步骤(1)获得的具有泛素化位点的肽的步骤。 (3)获得的消化材料。

    Pharmacological profiling of drugs with cell-based assays
    3.
    发明公开
    Pharmacological profiling of drugs with cell-based assays 审中-公开
    用基于细胞的测定法对药物进行药理分析

    公开(公告)号:EP2363496A1

    公开(公告)日:2011-09-07

    申请号:EP10015840.1

    申请日:2005-08-18

    IPC分类号: C12Q1/02 G01N33/50

    摘要: The instant invention provides a method for establishing safety profiles for chemical compounds, as well as pharmacological profiling said method comprising (A) testing the effects of said chemical compounds on the amount and/or post-translational modifications of two or more macromolecules in intact cells; (B) constructing a pharmacological profile based on the results of said tests; and (C) comparing said profile to the profile(s) of drugs with established safety characteristics. Additionally, the invention is also directed to a composition comprising an assay panel, said panel comprising at least one high-content assay for the amount and/or post-translational modification of a protein and at least one high-content assay for the amount and/or subcellular location of a protein-protein interaction.

    摘要翻译: 本发明提供了建立化学化合物安全性概况的方法以及药理概况分析,所述方法包括(A)测试所述化学化合物对完整细胞中两种或更多种大分子的量和/或翻译后修饰的影响 ; (B)基于所述测试的结果构建药理学特征; 和(C)将所述特征与具有确定安全特征的药物特征进行比较。 此外,本发明还涉及包含测定组的组合物,所述组包含至少一种蛋白质的量和/或翻译后修饰的高含量测定和至少一种高含量测定的量以及 /或蛋白质 - 蛋白质相互作用的亚细胞定位。

    HISTONE PROTEIN UBIQUITINATION AS A CANCER BIOMARKER
    7.
    发明公开
    HISTONE PROTEIN UBIQUITINATION AS A CANCER BIOMARKER 有权
    作为癌症生物标记物的组织定位

    公开(公告)号:EP2638394A4

    公开(公告)日:2014-06-18

    申请号:EP11839316

    申请日:2011-11-14

    摘要: The present disclosure relates generally to the field of cancer diagnosis. More specifically, the present disclosure relates to the identification and use of monoubiquitination of histone 2B as a biomarker for the diagnosis and prognosis of cancer including, but not limited to, parathyroid cancer. The present disclosure also relates to the identification of binding between CDC73 and RNF20, and the use of CDC73 and RNF20 in an assay for screening for an agent that modulates monoubiquitination of a histone protein.

    摘要翻译: 本公开一般涉及癌症诊断领域。 更具体地,本公开涉及组蛋白2B的单泛素化作为用于诊断和预后的癌症的生物标志物的鉴定和用途,包括但不限于甲状旁腺癌。 本公开还涉及鉴定CDC73和RNF20之间的结合,以及CDC73和RNF20在用于筛选调节组蛋白的单泛素化的试剂的测定中的用途。

    PHARMACOLOGICAL PROFILING OF DRUGS WITH CELL-BASED ASSAYS
    9.
    发明公开
    PHARMACOLOGICAL PROFILING OF DRUGS WITH CELL-BASED ASSAYS 审中-公开
    CREATING原料药的药理特性文件通过试验对蜂窝基站的方式

    公开(公告)号:EP1784642A2

    公开(公告)日:2007-05-16

    申请号:EP05788134.4

    申请日:2005-08-18

    IPC分类号: G01N33/53

    摘要: The instant invention provides a method for establishing safety profiles for chemical compounds, as well as pharmacological profiling said method comprising (A) testing the effects of said chemical compounds on the amount and/or post-translational modifications of two or more macromolecules in intact cells; (B) constructing a pharmacological profile based on the results of said tests; and (C) comparing said profile to the profile(s) of drugs with established safety characteristics. Additionally, the invention is also directed to a composition comprising an assay panel, said panel comprising at least one high-content assay for the amount and/or post-­translational modification of a protein and at least one high-content assay for the amount and/or subcellular location of a protein-protein interaction.