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Improved Nucleic Acid Triggered Probe Activation through the Use of a 5-Thiomethyluracil Peptide Nucleic Acid Building Block

机译:通过使用5-硫代甲基尿嘧啶肽核酸构建基块改善核酸触发的探针激活

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摘要

To improve the efficiency of a nucleic acid triggered probe activation(NATPA)system a 5-thiomethyluracil peptide nucleic acid(PNA)building block has been synthesized.Attachment of imidazole and a coumarin ester to uracils at the ends of two PNAs resulted in a 550 000-fold acceleration of DNA-triggered coumarin release relative to imidazole and a 6-fold increase in k_cat relative to a system which had these groups attached to the amino and carboxy ends of PNAs.
机译:为了提高核酸触发探针激活(NATPA)系统的效率,合成了5-硫代甲基尿嘧啶肽核酸(PNA)构件。将咪唑和香豆素酯连接到两个PNA末端的尿嘧啶上产生了550相对于咪唑,DNA引发的香豆素释放速度提高了000倍,而k_cat相对于将这些基团连接到PNA氨基和羧基末端的系统,k_cat增长了6倍。

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  • 来源
    《Organic letters》 |2005年第5期|p.751-754|共4页
  • 作者单位

    Department of Chemistry,Washington University,One Brookings Drive,St.Louis,Missouri 63130;

    Department of Chemistry,Washington University,One Brookings Drive,St.Louis,Missouri 63130;

    Department of Chemistry,Washington University,One Brookings Drive,St.Louis,Missouri 63130;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 有机化学;
  • 关键词

  • 入库时间 2022-08-18 00:01:57

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