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开发一种分裂 SNAP-CLIP 双重标记系统,用于追踪活细胞中从蛋白质-蛋白质复合物解离后的蛋白质。

Development of a Split SNAP-CLIP Double Labeling System for Tracking Proteins Following Dissociation from Protein-Protein Complexes in Living Cells.

机构信息

Department of Life Science and Technology, School of Life Science and Technology, Tokyo Institute of Technology . 4259 Nagatsuta, Midori-ku, Yokohama 226-8502, Japan.

出版信息

Anal Chem. 2016 Aug 16;88(16):8166-71. doi: 10.1021/acs.analchem.6b01906. Epub 2016 Aug 3.

Abstract

The split SNAP-tag protein-fragment complementation assay (PCA) is a useful tool for imaging protein-protein interactions (PPIs) in living cells. In contrast to conventional methods employed for imaging PPIs, the split SNAP-tag PCA enables tracking of proteins following dissociation from protein-protein complexes. A limitation of this system, however, is that it only allows for labeling and tracking of one of the proteins forming the protein-protein complex. To track both proteins forming a protein-protein complex, each protein needs to be appropriately labeled. In this study, a split SNAP-CLIP double labeling system is developed and applied for tracking of each protein forming a protein-protein complex. As a proof-of concept, FM protein for PPIs and protein kinase C alpha (PKCα) for translocation are introduced to a split SNAP-CLIP double labeling system. The results show a split SNAP-CLIP double labeling system enables labeling of both proteins in a protein-protein complex and subsequent tracking of each of the proteins following dissociation from the protein-protein complexes in living cells.

摘要

分裂的 SNAP 标签蛋白片段互补测定法(PCA)是一种用于在活细胞中成像蛋白质-蛋白质相互作用(PPIs)的有用工具。与用于成像 PPIs 的传统方法相比,分裂的 SNAP 标签 PCA 允许在从蛋白质-蛋白质复合物解离后追踪蛋白质。然而,该系统的一个限制是,它仅允许对形成蛋白质-蛋白质复合物的一种蛋白质进行标记和追踪。要追踪形成蛋白质-蛋白质复合物的两种蛋白质,每种蛋白质都需要进行适当的标记。在这项研究中,开发了一种分裂的 SNAP-CLIP 双重标记系统,并将其应用于追踪形成蛋白质-蛋白质复合物的每种蛋白质。作为概念验证,将 FM 蛋白用于 PPIs 和蛋白激酶 Cα(PKCα)用于易位引入到分裂的 SNAP-CLIP 双重标记系统中。结果表明,分裂的 SNAP-CLIP 双重标记系统能够标记蛋白质-蛋白质复合物中的两种蛋白质,并在活细胞中从蛋白质-蛋白质复合物解离后追踪每种蛋白质。

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