4.6 Article

Rapid and Specific Post-Synthesis Modification of DNA through a Biocompatible Condensation of 1,2-Aminothiols with 2-Cyanobenzothiazole

期刊

CHEMISTRY-A EUROPEAN JOURNAL
卷 19, 期 12, 页码 4036-4042

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/chem.201201677

关键词

bioorthogonal reactions; click chemistry; cyanobenzothiazole; DNA; post-synthesis modification

资金

  1. Molecular Basis of Disease Program at Georgia State University
  2. GSU University
  3. National Institutes of Health [GM086925, GM084933]

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Post-synthesis modification of DNA is an important way of functionalizing DNA molecules. Herein, we describe a method that first enzymatically incorporates a cyanobenzothiazole (CBT)-modified thymidine. The side-chain handle CBT can undergo a rapid and site-specific cyclization reaction with 1,2-aminothiols to afford DNA functionalization in aqueous solution. Another key advantage of this method is the formation of a single stereo/regioisomer in the process, which allows for precise control of DNA modification to yield a single component for aptamer selection work and other applications.

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