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首页> 外文期刊>Molecules >Binding of Small Molecules to G-quadruplex DNA in Cells Revealed by Fluorescence Lifetime Imaging Microscopy of o-BMVC Foci
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Binding of Small Molecules to G-quadruplex DNA in Cells Revealed by Fluorescence Lifetime Imaging Microscopy of o-BMVC Foci

机译:小分子对荧光寿命显微镜显微镜显微镜揭示的细胞中的小分子与Quadrepled DNA的结合

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摘要

G-quadruplex (G4) structures have recently received increasing attention as a potential target for cancer research. We used time-gated fluorescence lifetime imaging microscopy (FLIM) with a G4 fluorescent probe, 3,6-bis(1-methyl-2-vinylpyridinium) carbazole diiodide (o-BMVC), to measure the number of o-BMVC foci, which may represent G4 foci, in cells as a common signature to distinguish cancer cells from normal cells. Here, the decrease in the number of o-BMVC foci in the pretreatment of cancer cells with TMPyP4, BRACO-19 and BMVC4 suggested that they directly bind to G4s in cells. In contrast, the increase in the number of o-BMVC foci in the pretreatment of cells with PDS and Hoechst 33258 (H33258) suggested that they do not inhabit the binding site of o-BMVC to G4s in cells. After the H33258 was removed, the gradual decrease of H33258-induced G4 foci may be due to DNA repair. The purpose of this work is to introduce o-BMVC foci as an indicator not only to verify the direct binding of potential G4 ligands to G4 structures but also to examine the possible effect of some DNA binding ligands on DNA integrity by monitoring the number of G4 foci in cells.
机译:G-Quadruplex(G4)结构最近接受了对癌症研究的潜在目标的影响。我们使用时隙荧光寿命成像显微镜(FLIM)与G4荧光探针,3,6-双(1-甲基-2-乙烯基吡啶)咔唑二碘酰基(O-BMVC),以测量O-BMVC焦点的数量,这可以代表G4焦点,在细胞中作为常见的签名,以区分癌细胞与正常细胞。这里,用TMPYP4,Braco-19和BMVC4预处理癌细胞预处理中O-BMVC焦点的数量的降低表明它们与细胞中的G4s直接结合。相反,具有PDS和Hoechst 33258(H33258)预处理细胞的O-BMVC焦点的数量增加(H33258)表明它们不栖息于细胞中O-BMVC至G4s的结合位点。除去H33258后,H33258诱导的G4焦点的逐渐减少可能是由于DNA修复。这项工作的目的是将O-BMVC焦点引入作为指示器,不仅可以通过监测G4的数量来检查一些DNA结合配体对DNA完整性对DNA完整性的可能效果焦点在细胞中。

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