Institute of Atomic and Molecular Sciences, Academia Sinica, Taipei 106, Taiwan.
Molecules. 2020 Sep 7;25(18):4083. doi: 10.3390/molecules25184083.
Identification of the existence of G-quadruplex (G4) structure, from a specific G-rich sequence in cells, is critical to the studies of structural biology and drug development. Accumulating evidence supports the existence of G4 structure in vivo. Particularly, time-gated fluorescence lifetime imaging microscopy (FLIM) of a G4 fluorescent probe, 3,6-bis(1-methyl-2-vinylpyridinium) carbazole diiodide (-BMVC), was used to quantitatively measure the number of G4 foci, not only in different cell lines, but also in tissue biopsy. Here, circular dichroism spectra and polyacrylamide gel electrophoresis assays show that the use of antisense oligonucleotides unfolds their G4 structures in different percentages. Using antisense oligonucleotides, quantitative measurement of the number of -BMVC foci in time-gated FLIM images provides a method for identifying which G4 motifs form G4 structures in fixed cells. Here, the decrease of the -BMVC foci number, upon the pretreatment of antisense sequences, (CCCTAA)CCCTA, in fixed cells and at the end of metaphase chromosomes, allows us to identify the formation of telomeric G4 structures from TTAGGG repeats in fixed cells.
鉴定细胞中特定的富含 G 序列是否存在 G-四链体 (G4) 结构,对于结构生物学和药物开发的研究至关重要。越来越多的证据支持 G4 结构在体内的存在。特别是,G4 荧光探针 3,6-双(1-甲基-2-乙烯基吡啶鎓)咔唑二碘化物(-BMVC)的时间门控荧光寿命成像显微镜(FLIM)被用于定量测量 G4 焦点的数量,不仅在不同的细胞系中,而且在组织活检中也是如此。这里,圆二色光谱和聚丙烯酰胺凝胶电泳实验表明,反义寡核苷酸的使用以不同的百分比展开其 G4 结构。使用反义寡核苷酸,通过时间门控 FLIM 图像对 -BMVC 焦点数量进行定量测量,提供了一种方法来识别固定细胞中形成 G4 结构的 G4 基序。在这里,预处理反义序列(CCCTAA)CCCTA 后,固定细胞中和中期染色体末期 -BMVC 焦点数量的减少,使我们能够识别固定细胞中 TTAGGG 重复序列形成端粒 G4 结构。