Engineering yellow fluorescent protein probe for visualization of parallel DNA G-quadruplex

T. Truong, Trang T P Phan, Linh Le, D. Nguyen, H. Nguyen, D. T. Dang
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引用次数: 1

Abstract

Introduction: The formation of G-quadruplex plays a key role in many biological processes. Therefore, visualization of G-quadruplex is highly essential for design of G-quadruplex-targeted small molecules (drugs). Herein, we report on an engineered fluorescent protein probe which was able to distinguish G-quadruplex topologies. Methods: The fluorescent protein probe was generated by genetically incorporating yellow fluorescent protein (YFP) to RNA helicase associated with AU-rich element (RHAU) peptide motif. Results: This probe could selectively bind and visualize parallel G-quadruplex structure (T95-2T) at high affinity (Kd~130 nM). Visualization of the parallel G-quadruplex by RHAU-YFP could be easily observed in vitro by using normal Gel Doc or the naked eye. Conclusion: The YFP probe could be encoded in cells to provide a powerful tool for detection of parallel G-quadruplexes both in vitro and in vivo.  
工程黄色荧光蛋白探针显示平行DNA g -四重体
g -四重体的形成在许多生物过程中起着关键作用。因此,g -四聚体的可视化对于g -四聚体靶向小分子(药物)的设计至关重要。在此,我们报道了一种工程荧光蛋白探针,它能够区分g -四重体拓扑结构。方法:将黄色荧光蛋白(YFP)与富au元素(RHAU)肽基序相关的RNA解旋酶基因结合,制备荧光蛋白探针。结果:该探针能以高亲和力(Kd~130 nM)选择性结合并可视化平行g -四联体结构(T95-2T)。通过正常凝胶或肉眼观察,RHAU-YFP可以很容易地在体外观察到平行g -四联体的可视化。结论:YFP探针可在细胞内编码,为体外和体内平行g -四联体的检测提供了强有力的工具。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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