Department of Chemistry, Humboldt University of Berlin, Brook-Taylor-Str. 2, 12489 Berlin, Germany.
J Am Chem Soc. 2022 Jun 22;144(24):10700-10704. doi: 10.1021/jacs.2c03188. Epub 2022 Jun 13.
Nucleic-acid-templated chemical reactions are currently explored for applications in DNA-encoded drug discovery, nucleic acid diagnostics, and theranostics. Of particular interest are reactions enabling the template to gain catalytic activity, so that enzymatic amplification of low copy targets would no longer be necessary. Herein, we introduce a new reaction design relying on the template-controlled cleavage of PNA-spermine conjugates. With turnover frequencies in the range of 3-10 min and a / = 1.3 × 10 M s, the loss of affinity upon reaction provides a catalytic efficiency equal to most enzymatic conversions and superior to nucleic-acid-templated reactions reported to date.
核酸模板化学反应用于 DNA 编码药物发现、核酸诊断和治疗学等领域。特别感兴趣的是能够使模板获得催化活性的反应,从而不再需要对低拷贝目标进行酶促扩增。本文中,我们引入了一种新的反应设计,依赖于 PNA-精脒缀合物的模板控制切割。其周转率在 3-10 min 范围内,a = 1.3×10 M s,反应时亲和力的丧失提供了与大多数酶转化相当的催化效率,优于迄今为止报道的核酸模板反应。