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Fluorescence resonance energy transfer-based technologies in the study of protein-protein interactions at the cell surface

机译:基于荧光共振能量转移的技术研究细胞表面蛋白质间的相互作用

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Understanding of the molecular mechanisms of protein-protein interactions (PPIs) at the cell surface of living cells is fundamental to comprehend the functional meaning of a large number of cellular processes. Here we discuss how new methodological strategies derived from non-invasive fluorescence-based approaches (i.e. fluorescence resonance energy transfer, FRET) have been successfully developed to characterize plasma membrane PPIs. Importantly, these technologies alone - or in concert with complementary methods (i.e. SNAP-tag/TR-FRET, TIRF/FRET) - can become extremely powerful approaches for visualizing cell surface PPIs, even between more than two proteins and also in native tissues. Interestingly, these methods would also be relevant in drug discovery in order to develop new high-throughput screening approaches or to identify new therapeutic targets. Accordingly, herein we provide a thorough assessment on all biotechnological aspects, including strengths and weaknesses, of these fluorescence-based methodologies when applied in the study of PPIs occurring at the cell surface of living cells.
机译:理解活细胞细胞表面的蛋白质-蛋白质相互作用(PPI)的分子机制对于理解大量细胞过程的功能意义至关重要。在这里,我们讨论如何成功开发出基于非侵入式荧光方法的新方法论策略(即荧光共振能量转移,FRET)来表征质膜PPI。重要的是,这些技术本身-或与补充方法(即SNAP标签/ TR-FRET,TIRF / FRET)配合使用-甚至可以成为可视化细胞表面PPI的强大方法,甚至在两种以上的蛋白质之间以及在天然组织中也是如此。有趣的是,这些方法也将与药物发现相关,以开发新的高通量筛选方法或确定新的治疗靶标。因此,在本文中,当将这些基于荧光的方法应用于研究在活细胞的细胞表面发生的PPI时,我们对所有这些生物技术方面,包括优点和缺点,进行了全面的评估。

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