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Development of a New Method for Synthesis of Tandem Hairpin Pyrrole-Imidazole Polyamide Probes Targeting Human Telomeres

机译:靶向人端粒的串联发夹式吡咯-咪唑聚酰胺探针合成新方法的开发

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摘要

Pyrrole-imidazole (PI) polyamides bind to the minor groove of DNA in a sequence-specific manner without causing denaturation of DNA. To visualize telomeres specifically, tandem hairpin PI polyamides conjugated with a fluorescent dye have been synthesized, but the study of telomeres using these PI polyamides has not been reported because of difficulties synthesizing these tandem hairpin PI polyamides. To synthesize tandem hairpin PI polyamides more easily, we have developed new PI polyamide fragments and have used them as units in Fmoc solid-phase peptide synthesis. Using this new method, we synthesized four fluorescent polyamide probes for the human telomeric repeat TTAGGG, and we examined the binding affinities and specificities of the tandem hairpin PI polyamides, the UV-vis absorption and fluorescence spectra of the fluorescent polyamide probes, and telomere staining in mouse MC12 and human HeLa cells. The polyamides synthesized using the new method successfully targeted to human and mouse telomeres under mild conditions and allow easier labeling of telomeres in the cells while maintaining the telomere structure. Using the fluorescent polyamides, we demonstrated that the telomere length at a single telomere level is related to the abundance of TRF1 protein, a shelterin complex component in the telomere.
机译:吡咯-咪唑(PI)聚酰胺以序列特异性方式与DNA的小沟结合,而不会引起DNA变性。为了具体地观察端粒,已经合成了与荧光染料缀合的串联发夹PI聚酰胺,但是由于合成这些串联发夹PI聚酰胺的困难,尚未报道使用这些PI聚酰胺进行端粒的研究。为了更轻松地合成串联发夹式PI聚酰胺,我们开发了新的PI聚酰胺片段并将其用作Fmoc固相肽合成中的单元。使用这种新方法,我们合成了用于人类端粒重复序列TTAGGG的四种荧光聚酰胺探针,并研究了串联发夹PI聚酰胺的结合亲和力和特异性,荧光聚酰胺探针的UV-vis吸收和荧光光谱以及端粒染色在小鼠MC12和人类HeLa细胞中。使用该新方法合成的聚酰胺在温和条件下成功地靶向人和小鼠端粒,并允许在维持端粒结构的同时更轻松地标记细胞中的端粒。使用荧光聚酰胺,我们证明了单个端粒水平上的端粒长度与TRF1蛋白(端粒中的庇护素复合物成分)的丰度有关。

著录项

  • 来源
    《Journal of the American Chemical Society》 |2013年第44期|16468-16477|共10页
  • 作者单位

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan;

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan;

    Biological Macromolecules Laboratory, Structural Biology Center, National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan;

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan;

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan;

    Biological Macromolecules Laboratory, Structural Biology Center, National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan,Department of Genetics, School of Life Science, Graduate University for Advanced Studies (Sokendai), Mishima, Shizuoka 411-8540, Japan;

    Department of Chemistry, Graduate School of Science, Kyoto University, Sakyo, Kyoto 606-8502, Japan,institute for Integrated Cell-Material Science (WPI-iCeMS), Kyoto University, Sakyo, Kyoto 606-8501, Japan,Core Research for Evolutional Science and Technology (CREST), Japan Science and Technology Corporation (JST), Sanbancho, Chiyoda-ku, Tokyo 102-0075, Japan;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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  • 正文语种 eng
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  • 入库时间 2022-08-18 03:12:54

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