Sakamoto Satoshi, Tamura Takashi, Furukawa Takako, Komatsu Yasuo, Ohtsuka Eiko, Kitamura Masaya, Inoue Hideo
Department of Applied and Bioapplied Chemistry, Graduate School of Engineering, Osaka City University, Sugimoto 3-3-138, Sumiyoshi-ku, Osaka 558-8585, Japan.
Nucleic Acids Res. 2003 Mar 1;31(5):1416-25. doi: 10.1093/nar/gkg238.
Based on our recent studies of RNA cleavage by oligonucleotide-terpyridine.Cu(II) complex 5'- and/or 3'-conjugates, we designed 2'-O-methyloligonucleotides with two terpyridine-attached nucleosides at contiguous internal sites. To connect the 2'-terpyridine-modified uridine residue at the 5'-side to the 5'-O-terpyridyl nucleoside residue at the 3'-side, a dimethoxytrityl derivative of 5-hydroxypropyl-5'-O-terpyridyl-2'-deoxyuridine-3'-phosphoramidite was newly synthesized. Using this unit, we constructed two terpyridine conjugates, with either an unusual phophodiester bond or the bond extended by a propanediol(s)-containing linker. Cleavage reactions of the target RNA oligomer, under the conditions of conjugate excess in the presence of Cu(II), indicated that the conjugates precisely cleaved the RNA at the predetermined site and that one propanediol-containing linker was the most appropriate for inducing high cleavage activity. Furthermore, a comparison of the activity of the propanediol agent with those of the control conjugates with one complex confirmed that the two complexes are required for efficient RNA cleavage. The reaction of the novel cleaver revealed a bell-shaped pH-rate profile with a maximum at pH approximately 7.5, which is a result of the cooperative action of the complexes. In addition, we demonstrated that the agent catalytically cleaves an excess of the RNA, with the kinetic parameter kcat/K(m) = 0.118 nM(-1) x h(-1).
基于我们最近对寡核苷酸 - 三联吡啶·铜(II)配合物5'-和/或3'-缀合物进行RNA切割的研究,我们设计了在相邻内部位点带有两个连接三联吡啶的核苷的2'-O-甲基寡核苷酸。为了将5'-侧的2'-三联吡啶修饰的尿苷残基与3'-侧的5'-O-三联吡啶核苷残基连接起来,新合成了5-羟丙基-5'-O-三联吡啶-2'-脱氧尿苷-3'-亚磷酰胺的二甲氧基三苯甲基衍生物。使用这个单元,我们构建了两种三联吡啶缀合物,一种具有不寻常的磷酸二酯键,另一种通过含丙二醇的接头延长了键。在Cu(II)存在下共轭物过量的条件下,对目标RNA寡聚物的切割反应表明,共轭物在预定位点精确切割RNA,并且一个含丙二醇的接头最适合诱导高切割活性。此外,将丙二醇试剂与一种配合物的对照缀合物的活性进行比较,证实高效RNA切割需要两种配合物。新型切割剂的反应显示出钟形的pH - 速率曲线,在pH约7.5处有最大值,这是配合物协同作用的结果。此外,我们证明该试剂能催化切割过量的RNA,动力学参数kcat/K(m)=0.118 nM(-1)×h(-1)。