Maruyama Hideto, Oikawa Ryota, Hayakawa Mayu, Takamori Shono, Kimura Yasuaki, Abe Naoko, Tsuji Genichiro, Matsuda Akira, Shuto Satoshi, Ito Yoshihiro, Abe Hiroshi
Faculty of Pharmaceutical Sciences, Hokkaido University, Kita-12, Nishi-6, Kita-ku, Sapporo 060-0812, Japan.
Department of Chemistry, Graduate School of Science, Nagoya University, Furo, Chikusa, Nagoya 464-8602, Japan.
Nucleic Acids Res. 2017 Jul 7;45(12):7042-7048. doi: 10.1093/nar/gkx459.
We developed a new approach for chemical ligation of oligonucleotides using the electrophilic phosphorothioester (EPT) group. A nucleophilic phosphorothioate group on oligonucleotides was converted into the EPT group by treatment with Sanger's reagent (1-fluoro-2,4-dinitrobenzene). EPT oligonucleotides can be isolated, stored frozen, and used for the ligation reaction. The reaction of the EPT oligonucleotide and an amino-modified oligonucleotide took place without any extra reagents at pH 7.0-8.0 at room temperature, and resulted in a ligation product with a phosphoramidate bond with a 39-85% yield. This method has potential uses in biotechnology and chemical biology.
我们开发了一种使用亲电硫代磷酸酯(EPT)基团进行寡核苷酸化学连接的新方法。通过用桑格试剂(1-氟-2,4-二硝基苯)处理,寡核苷酸上的亲核硫代磷酸酯基团被转化为EPT基团。EPT寡核苷酸可以被分离、冷冻保存,并用于连接反应。EPT寡核苷酸与氨基修饰的寡核苷酸在室温下pH 7.0 - 8.0的条件下无需任何额外试剂即可发生反应,生成具有氨基磷酸酯键的连接产物,产率为39 - 85%。该方法在生物技术和化学生物学中具有潜在用途。