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A fluorescence-based helicase assay: application to the screening of G-quadruplex ligands

机译:基于荧光的解旋酶测定:在筛选G四联体配体中的应用

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摘要

Helicases, enzymes that unwind DNA or RNA structure, are present in the cell nucleus and in the mitochondrion. Although the majority of the helicases unwind DNA or RNA duplexes, some of these proteins are known to resolve unusual structures such as G-quadruplexes (G4) in vitro. G4 may form stable barrier to the progression of molecular motors tracking on DNA. Monitoring G4 unwinding by these enzymes may reveal the mechanisms of the enzymes and provides information about the stability of these structures. In the experiments presented herein, we developed a reliable, inexpensive and rapid fluorescence-based technique to monitor the activity of G4 helicases in real time in a 96-well plate format. This system was used to screen a series of G4 structures and G4 binders for their effect on the Pif1 enzyme, a 5′ to 3′ DNA helicase. This simple assay should be adaptable to analysis of other helicases and G4 structures.
机译:解旋酶是解开DNA或RNA结构的酶,存在于细胞核和线粒体中。尽管大多数解旋酶解链DNA或RNA双链体,但已知其中一些蛋白质可在体外分辨异常结构,例如G-四链体(G4)。 G4可能对跟踪DNA的分子运动的发展形成稳定的障碍。监测这些酶释放的G4可能揭示酶的机制,并提供有关这些结构稳定性的信息。在本文介绍的实验中,我们开发了一种可靠,便宜且快速的基于荧光的技术,以96孔板形式实时监测G4解旋酶的活性。该系统用于筛选一系列G4结构和G4结合物对Pif1酶(一种5'至3'DNA解旋酶)的作用。这种简单的测定方法应适用于其他解旋酶和G4结构的分析。

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