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通过 DNA 模板连接实现钌(II)光催化剂的开启。

Turn On of a Ruthenium(II) Photocatalyst by DNA-Templated Ligation.

机构信息

Department of Organic Chemistry, NCCR Chemical Biology, Faculty of Science, University of Geneva, 30 Quai Ernest-Ansermet, 1205, Geneva, Switzerland.

出版信息

Chemistry. 2019 Jan 2;25(1):334-342. doi: 10.1002/chem.201804283. Epub 2018 Nov 19.

Abstract

Here, the synthesis of a Ru photocatalyst by light-directed oligonucleotide-templated ligation reaction is described. The photocatalyst was found to have tremendous potential for signal amplification with >15000 turnovers measured in 9 hours. A templated reaction was used to turn on the activity of this ruthenium(II) photocatalyst in response to a specific DNA sequence. The photocatalysis of the ruthenium(II) complex was harnessed to uncage a new precipitating dye that is highly fluorescent and photostable in the solid state. This reaction was used to discriminate between different DNA analytes based on localization of the precipitate as well as for in cellulo miRNA detection. Finally, a bipyridine ligand functionalized with two different peptide nucleic acid (PNA) sequences was shown to enable template-mediated ligation (turn on of the ruthenium(II) photocatalysis) and recruitment of substrate for templated photocatalysis.

摘要

这里描述了一种通过光导向寡核苷酸模板连接反应合成 Ru 光催化剂的方法。该光催化剂在 9 小时内测量到 >15000 次的循环,具有巨大的信号放大潜力。模板反应被用来激活这种钌(II)光催化剂的活性,以响应特定的 DNA 序列。利用钌(II)配合物的光催化作用,解笼出一种新的沉淀染料,该染料在固态下具有高荧光性和光稳定性。该反应可用于根据沉淀的定位区分不同的 DNA 分析物,以及用于细胞内 miRNA 的检测。最后,用两个不同的肽核酸(PNA)序列功能化的联吡啶配体被证明能够进行模板介导的连接(钌(II)光催化的开启)和底物的募集用于模板化光催化。

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