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双杂交抗体微图案分析揭示了细胞表面 MHC I 重链的特异性相互作用。

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

机构信息

Department of Life Sciences and Chemistry, Jacobs University, Bremen, Germany.

出版信息

Elife. 2018 Sep 5;7:e34150. doi: 10.7554/eLife.34150.

Abstract

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 interactions of MHC I proteins at the cell surface under controlled conditions and to define the involved protein conformations. Our results show that homotypic 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 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.

摘要

我们展示了一种基于抗体微图案的双杂交测定法,用于研究主要组织相容性复合体 I 类 (MHC I) 蛋白在细胞表面的蛋白-蛋白相互作用。抗标签和构象特异性抗体分别用于特异性捕获特定形式的 MHC I 蛋白,通过荧光显微镜进行位置和构象特异性分析。该测定法用于在受控条件下研究细胞表面 MHC I 蛋白的相互作用,并确定涉及的蛋白构象。我们的结果表明,同种型相互作用仅发生在 MHC I 游离重链之间,我们发现轻链从 MHC I 蛋白复合物解离是 MHC I 相互作用的条件。细胞表面这些 MHC I 蛋白-蛋白相互作用的功能作用需要进一步研究。我们提出了我们的双杂交测定法的未来技术发展,以进一步分析 MHC I 蛋白-蛋白相互作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/dfaa/6125123/19f31e6a43f2/elife-34150-fig1.jpg

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