Zlatev Ivan, Foster Donald J, Liu Jingxuan, Charisse Klaus, Brigham Benjamin, Parmar Rubina G, Jadhav Vasant, Maier Martin A, Rajeev Kallanthottathil G, Egli Martin, Manoharan Muthiah
Alnylam Pharmaceuticals , 300 Third Street, Cambridge, Massachusetts 02142, United States.
Department of Biochemistry, Vanderbilt University , Nashville, Tennessee 37232, United States.
ACS Chem Biol. 2016 Apr 15;11(4):953-60. doi: 10.1021/acschembio.5b00654. Epub 2016 Jan 13.
5'-Phosphorylation is a critical step in the cascade of events that leads to loading of small interfering RNAs (siRNAs) into the RNA-induced silencing complex (RISC) to elicit gene silencing. 5'-Phosphorylation of exogenous siRNAs is generally accomplished by a cytosolic Clp1 kinase, and in most cases, the presence of a 5'-monophosphate on synthetic siRNAs is not a prerequisite for activity. Chemically introduced, metabolically stable 5'-phosphate mimics can lead to higher metabolic stability, increased RISC loading, and higher gene silencing activities of chemically modified siRNAs. In this study, we report the synthesis of 5'-C-malonyl RNA, a 5'-monophosphate bioisostere. A 5'-C-malonyl-modified nucleotide was incorporated at the 5'-terminus of chemically modified RNA oligonucleotides using solid-phase synthesis. In vitro silencing activity, in vitro metabolic stability, and in vitro RISC loading of 5'-C-malonyl siRNA was compared to corresponding 5'-phosphorylated and 5'-nonphosphorylated siRNAs. The 5'-C-malonyl siRNAs showed sustained or improved in vitro gene silencing and high levels of Ago2 loading and conferred dramatically improved metabolic stability to the antisense strand of the siRNA duplexes. In silico modeling studies indicate a favorable fit of the 5'-C-malonyl group within the 5'-phosphate binding pocket of human Ago2MID domain.
5'-磷酸化是一系列导致小干扰RNA(siRNA)加载到RNA诱导沉默复合体(RISC)以引发基因沉默的事件级联中的关键步骤。外源siRNA的5'-磷酸化通常由胞质Clp1激酶完成,并且在大多数情况下,合成siRNA上5'-单磷酸的存在不是活性的先决条件。化学引入的、代谢稳定的5'-磷酸模拟物可导致更高的代谢稳定性、增加的RISC加载以及化学修饰siRNA更高的基因沉默活性。在本研究中,我们报道了5'-C-丙二酰RNA(一种5'-单磷酸生物电子等排体)的合成。使用固相合成法将5'-C-丙二酰修饰的核苷酸掺入化学修饰的RNA寡核苷酸的5'-末端。将5'-C-丙二酰siRNA的体外沉默活性、体外代谢稳定性和体外RISC加载与相应的5'-磷酸化和5'-非磷酸化siRNA进行比较。5'-C-丙二酰siRNA显示出持续或改善的体外基因沉默以及高水平的Ago2加载,并赋予siRNA双链体反义链显著改善的代谢稳定性。计算机模拟研究表明5'-C-丙二酰基团与人Ago2MID结构域的5'-磷酸结合口袋具有良好的契合度。