Unnatural base pairs mediate the site-specific incorporation of an unnatural hydrophobic component into RNA transcripts

被引:16
|
作者
Endo, M
Mitsui, T
Okuni, T
Kimoto, A
Hirao, I
Yokoyama, S
机构
[1] RIKEN, Prot Res Grp, Prot Synth Technol Team, Genomic Sci Ctr,Tsurumi Ku, Yokohama, Kanagawa 2300045, Japan
[2] RIKEN, Harima Inst, Sayo, Hyogo 6795148, Japan
[3] Univ Tokyo, Grad Sch Sci, Dept Biophys & Biochem, Bunkyo Ku, Tokyo 1130033, Japan
[4] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
关键词
unnatural base pair;
D O I
10.1016/j.bmcl.2004.02.072
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Site-specific incorporation of a hydrophobic nucleotide analog into RNA, by T7 transcription mediated by unnatural base pairs, was developed. The nucleotide analog, 5-phenylethynyl-3-(beta-D-ribofuranosyl)pyridin-2-one 5-triphosphate (denoted by Ph-yTP), was chemically synthesized and then site-specifically incorporated by T7 RNA polymerase into RNA opposite the pairing partner, 2-amino-6-(2-thienyl)purine (denoted by s) in DNA templates. The introduction of Ph-y into a theophylline-binding RNA aptamer, in which a uridine in the internal loop was replaced by Ph-y, raised the thermal stability of the aptamer. Thus, this unnatural nucleotide analog would be useful for stabilizing RNA tertiary structures and complexes between RNA and other molecules. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2593 / 2596
页数:4
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