Facile syntheses of BODIPY derivatives for fluorescent labeling of the 3′ and 5′ ends of RNAs

被引:46
作者
Ikawa, Yoshiya [1 ,2 ]
Moriyama, Shoji [1 ]
Furuta, Hiroyuki [1 ]
机构
[1] Kyushu Univ, Dept Chem & Biochem, Grad Sch Engn, Nishi Ku, Fukuoka 8190395, Japan
[2] Japan Sci & Technol Agcy, PRESTO, Kawaguchi, Saitama 3320012, Japan
关键词
BODIPY; fluorophore; imaging; labeling; RNA; ribozyme; Tetrahymena;
D O I
10.1016/j.ab.2008.03.054
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As inexpensive and readily available fluorophores for 3' and 5' end labeling of RNA molecules, symmetrical BODIPY (boron dipyrromethene: 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene) derivatives having a primary amino group were designed, and their facile synthetic route was established. Novel BODIPY derivatives exhibited photophysical properties comparable to commercially available BODIPY FL EDA (4,4-difluoro-5,7-dimethyl-4-bora-3 a,4a-diaza-s-indacene-3-propionyl ethylenediamine). To confirm utility of new derivatives, specific labeling of the 3' and 5' ends of in vitro transcribed RNAs was carried out. Furthermore, the 3 ' end of the 5 ' fragment of the bimolecular Tetrahymena ribozyme was labeled, and its catalytic activity was investigated. (C) 2008 Elsevier Inc. All rights reserved.
引用
收藏
页码:166 / 170
页数:5
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