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Facile analysis of protein-protein interactions in living cells by enriched visualization of the p-body

机译:通过丰富的p体可视化,轻松分析活细胞中的蛋白质-蛋白质相互作用

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Protein-Protein Interactions (PPIs) play essential roles in diverse biological processes and their misregulations are associated with a wide range of diseases. Especially, the growing attention to PPIs as a new class of therapeutic target is increasing the need for an efficient method of cell-based PPI analysis. Thus, we newly developed a robust PPI assay (SeePPI) based on the co-translocation of interacting proteins to the discrete subcellular compartment ‘processing body’ (p-body) inside living cells, enabling a facile analysis of PPI by the enriched fluorescent signal. The feasibility and strength of SeePPI (Signal enhancement exclusively on P-body for Protein-protein Interaction) assay was firmly demonstrated with FKBP12/FRB interaction induced by rapamycin within seconds in real-time analysis of living cells, indicating its recapitulation of physiological PPI dynamics. In addition, we applied p53/MDM2 interaction and its dissociation by Nutlin-3 to SeePPI assay and further confirmed that SeePPI was quantitative and well reflected the endogenous PPI. Our SeePPI assay will provide another useful tool to achieve an efficient analysis of PPIs and their modulators in cells.
机译:蛋白质-蛋白质相互作用(PPI)在多种生物过程中起着至关重要的作用,它们的调控异常与多种疾病有关。尤其是,人们越来越重视PPI作为一类新型的治疗靶标,因此越来越需要一种有效的基于细胞的PPI分析方法。因此,我们基于相互作用蛋白向活细胞内离散的亚细胞区室“加工体”(p-body)的共转运,新开发了一种功能强大的PPI分析(SeePPI),从而可以通过丰富的荧光信号轻松地分析PPI 。雷帕霉素诱导的FKBP12 / FRB相互作用可在数秒内对活细胞进行实时分析,从而牢固地证明了SeePPI(仅通过P体上的信号增强可实现蛋白-蛋白相互作用)测定的可行性和强度,表明了其对生理PPI动态的概括。另外,我们将p53 / MDM2的相互作用及其通过Nutlin-3的解离应用于SeePPI分析,并进一步证实SeePPI是定量的并很好地反映了内源PPI。我们的SeePPI分析将提供另一个有用的工具,以实现细胞中PPI及其调节剂的有效分析。

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