Department of Material and Life Chemistry, Faculty of Engineering, Kanagawa University , 3-27-1 Rokkakubashi, Kanagawa-ku, Yokohama 221-8686, Japan.
J Org Chem. 2017 Feb 3;82(3):1796-1802. doi: 10.1021/acs.joc.6b02527. Epub 2017 Jan 23.
An efficient conjugatable and bioreduction cleavable linker was designed and synthesized for the 5'-terminal ends of oligonucleotides. A phosphoramidite reagent bearing this linker was successfully applied to solid phase synthesis and incorporated at the 5'-terminal ends of oligonucleotides. The controlled pore glass (CPG)-supported oligonucleotides were subsequently conjugated to a diverse range of functional molecules using a CuAAC reaction. The synthesized oligonucleotide conjugates were then cleaved using a nitroreductase/NADH bioreduction system to release the naked oligonucleotides.
设计并合成了一种用于寡核苷酸 5'-末端的有效可共轭和生物还原可裂解连接子。带有该连接子的亚磷酰胺试剂成功地应用于固相合成,并被掺入到寡核苷酸的 5'-末端。随后,使用 CuAAC 反应将 CP 负载的寡核苷酸与各种功能分子连接。合成的寡核苷酸缀合物然后使用硝基还原酶/NADH 生物还原系统进行切割,以释放裸露的寡核苷酸。