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BINDINGZYME ARRAYS AND HIGH-THROUGHPUT PROTEOMIC METHODS

机译:结合酶阵列和高通量蛋白质组学方法

摘要

Provided herein are methods for identifying the presence or absence of a polypeptide variance between different biological samples and corresponding methods for generating a high-throughput screen to rapidly identify variances of one or more polypeptides in different biological samples. In particular, a variance in a post-translational modification on a particular polypeptide in the biological samples can be identified, such as the presence or absence of a polypeptide having an attached phosphoryl moiety, for example. In these methods, a catalytically inactivated enzyme (i.e. bindingzyme) is utilized as a substrate-specific binding protein. These bindingzymes can bind to one or more substrates in biological samples and a bound substrate can act as a marker to distinguish one sample from another. These methods also are useful for isolating substrates for their identification, for the detection of substrates in a sample, and for the discovery and development of ethical drugs.
机译:本文提供了用于鉴定在不同生物样品之间存在或不存在多肽变异的方法,以及用于生成高通量筛选以快速鉴定在不同生物样品中一种或多种多肽的变异的相应方法。特别地,可以鉴定生物样品中特定多肽的翻译后修饰的变化,例如,存在或不存在具有连接的磷酰基部分的多肽。在这些方法中,催化失活的酶(即结合酶)被用作底物特异性结合蛋白。这些结合酶可以结合生物样品中的一种或多种底物,并且结合的底物可以充当将一个样品与另一个样品区分开的标记。这些方法还可用于分离底物以进行鉴定,检测样品中的底物以及发现和开发道德药物。

著录项

  • 公开/公告号EP1578961A4

    专利类型

  • 公开/公告日2006-08-30

    原文格式PDF

  • 申请/专利权人 RODI PHARMA INC.;

    申请/专利号EP20030800419

  • 发明设计人 RODI CHARLIE;

    申请日2003-12-31

  • 分类号C12N9/00;C12N11/00;G01N33/53;

  • 国家 EP

  • 入库时间 2022-08-21 21:29:38

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