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high-throughput screening method for measuring the activity of gap junctional intercellular communication

机译:间隙连接细胞间通讯活性的高通量筛选方法

摘要

The present invention relates to a high-speed screening method for measuring a gap junction activity between a donor cell expressing an iodide transporter and a receptor cell expressing an iodide sensor fluorescent protein, (iodide) transporter membrane protein and iodide sensor YFP QL protein is co-cultured with iodide, iodide enters the donor cell and passes through the gap junction to the receptor cell And the transferred iodide can bind to the YFP QL protein to quench the fluorescence and it can be confirmed that the change in the activity of the gap junction can be sensitively and quickly measured by measuring the iodide. A method for measuring the intercellular gap junction activity of a drug screening chamber using a gap junction activity regulator To be useful. In addition, since the method of measuring the gap junction activity of the present invention can be applied to a cell expressing a connexin protein which is a tube protein forming a gap junction, it has a wide range of application fields and a Z 'value (Z'factor ), It is effective as an ultrafast screening analysis.
机译:本发明涉及一种用于测量表达碘化物转运蛋白的供体细胞与表达碘化物传感器荧光蛋白,(碘化物)转运蛋白膜蛋白和碘化物传感器YFP QL的受体细胞之间的间隙连接活性的高速筛选方法。 蛋白与碘化物共培养,碘化物进入供体细胞并通过间隙连接到达受体细胞,转移的碘化物可以与YFP QL 蛋白结合从而猝灭荧光,可以确认,通过测量碘化​​物,可以灵敏且快速地测量间隙连接的活性变化。一种使用间隙连接活性调节剂来测量药物筛选室的细胞间间隙连接活性的方法。另外,由于本发明的测量间隙连接活性的方法可以应用于表达连接蛋白的细胞,所述连接蛋白是形成间隙连接的管蛋白,因此其具有广泛的应用领域和Z'值( Z'factor),作为超快速筛选分析是有效的。

著录项

  • 公开/公告号KR101818850B1

    专利类型

  • 公开/公告日2018-01-16

    原文格式PDF

  • 申请/专利权人 연세대학교 산학협력단;

    申请/专利号KR20160049447

  • 发明设计人 이진우;이주연;최은주;

    申请日2016-04-22

  • 分类号G01N33/50;G01N33/58;G01N33/68;

  • 国家 KR

  • 入库时间 2022-08-21 12:38:35

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