Hennig Mirko, Scott Lincoln G, Sperling Edit, Bermel Wolfgang, Williamson James R
Department of Biochemistry and Molecular Biology, Medical University of South Carolina, 173 Ashley Avenue, P.O. Box 250509, Charleston, South Carolina 29425, USA.
J Am Chem Soc. 2007 Dec 5;129(48):14911-21. doi: 10.1021/ja073825i. Epub 2007 Nov 9.
Enzymatic synthesis methods for the fluorinated 5'-triphosphate analogues 5F-UTP and 5F-CTP have been developed to facilitate 19F-labeling of RNAs for biophysical studies. HIV-2 TAR RNAs were synthesized using these analogues by in vitro transcription reactions using T7 RNA polymerase. The uniform incorporation of 5F-U or 5F-C analogues into HIV-2 TAR RNA transcripts does not significantly alter the RNA structure or thermodynamic stability. Fluorine observed homonuclear 19F-19F and heteronuclear 19F-1H NOE experiments providing selective distance information are presented and discussed. The availability of efficient synthesis of 5F-UTP, and for the first time, 5F-CTP, will facilitate the use of 5F-labeled RNAs in structural, ligand binding, and dynamic studies of RNAs using the advantages of 19F-labeling.
已开发出用于氟化5'-三磷酸类似物5F-UTP和5F-CTP的酶促合成方法,以促进用于生物物理研究的RNA的19F标记。使用这些类似物通过T7 RNA聚合酶的体外转录反应合成了HIV-2 TAR RNA。将5F-U或5F-C类似物均匀掺入HIV-2 TAR RNA转录本中不会显著改变RNA结构或热力学稳定性。本文展示并讨论了氟观察到的提供选择性距离信息的同核19F-19F和异核19F-1H NOE实验。5F-UTP以及首次实现的5F-CTP的高效合成,将利用19F标记的优势,促进5F标记的RNA在RNA的结构、配体结合和动力学研究中的应用。