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A two-hybrid antibody micropattern assay reveals specific in cis interactions of MHC I heavy chains at the cell surface

机译:两种杂交抗体微模式分析揭示了细胞表面MHC I重链的顺式相互作用特异性

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摘要

We demonstrate a two-hybrid assay based on antibody micropatterns to study protein-protein interactions at the cell surface of major histocompatibility complex class I (MHC I) proteins. Anti-tag and conformation-specific antibodies are used for individual capture of specific forms of MHC I proteins that allow for location- and conformation-specific analysis by fluorescence microscopy. The assay is used to study the in cis interactions of MHC I proteins at the cell surface under controlled conditions and to define the involved protein conformations. Our results show that homotypic in cis interactions occur exclusively between MHC I free heavy chains, and we identify the dissociation of the light chain from the MHC I protein complex as a condition for MHC I in cis interactions. The functional role of these MHC I protein-protein interactions at the cell surface needs further investigation. We propose future technical developments of our two-hybrid assay for further analysis of MHC I protein-protein interactions.
机译:我们展示了一种基于抗体微模式的双杂交试验,以研究主要组织相容性复合体I类(MHC I)主要细胞表面的蛋白质-蛋白质相互作用。抗标签和构象特异性抗体可用于捕获特定形式的MHC I蛋白,从而可以通过荧光显微镜进行位置和构象特异性分析。该测定法用于研究在受控条件下细胞表面MHC I蛋白的顺式相互作用,并确定涉及的蛋白构象。我们的结果表明,顺式相互作用的同型性仅在MHC I自由重链之间发生,并且我们确定MHC I蛋白复合物中轻链的解离是MHC I顺式相互作用的条件。这些MHC I蛋白-蛋白相互作用在细胞表面的功能作用需要进一步研究。我们提出了进一步的MHC I蛋白质-蛋白质相互作用分析的两杂交法技术发展的建议。

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