4.8 Article

Alkene-Tetrazine Ligation for Imaging Cellular DNA

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 53, 期 35, 页码 9168-9172

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201403580

关键词

bioorthogonal reporters; Diels-Alder cycloaddition; fluorescent probes; metabolic labeling; nucleosides

资金

  1. Swiss National Science Foundation [146754]
  2. University of Zurich Forschungskredit [FK-13-113]

向作者/读者索取更多资源

5-Vinyl-2'-deoxyuridine (VdU) is the first reported metabolic probe for cellular DNA synthesis that can be visualized by using an inverse electron demand Diels-Alder reaction with a fluorescent tetrazine. VdU is incorporated by endogenous enzymes into the genomes of replicating cells, where it exhibits reduced genotoxicity compared to 5-ethynyl-2'-deoxyuridine (EdU). The VdU-tetrazine ligation reaction is rapid (k approximate to 0.02m(-1) s(-1)) and chemically orthogonal to the alkyne-azide click reaction of EdU-modified DNA. Alkene-tetrazine ligation reactions provide the first alternative to azide-alkyne click reactions for the bioorthogonal chemical labeling of nucleic acids in cells and facilitate time-resolved, multicolor labeling of DNA synthesis.

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