Studies on aminoisonucleoside modified siRNAs: Stability and silencing activity

被引:11
作者
Li, Zong-Sheng
Qiao, Ren-Ping
Du, Quan
Yang, Zhen-Jun
Zhang, Liang-Ren
Zhang, Pei-Zhuo
Liang, Zi-Cai
Zhang, Li-He [1 ]
机构
[1] Peking Univ, Sch Pharmaceut Sci, State Key Lab Nat & Biomimet Drugs, Beijing 100083, Peoples R China
[2] Peking Univ, Inst Mol Med, Beijing 100871, Peoples R China
[3] Shanghai GenePharma Co Ltd, ZJ High Tech Pk, Shanghai 201203, Peoples R China
关键词
SMALL INTERFERING RNA; CHEMICAL-MODIFICATIONS; MAMMALIAN-CELLS; IN-VITRO; OLIGONUCLEOTIDES; OLIGODEOXYNUCLEOTIDES; HYBRIDIZATION; RECOGNITION; DUPLEXES; COMPLEX;
D O I
10.1021/bc060398+
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
A novel class of aminoisonucleoside was synthesized and incorporated into a luciferase gene-targeting siRNA. Structural and functional analyses of such a kind of siRNAs indicated that sense strand modifications with aminoisonucleoside at the 3' or 5' terminal, such as ssIso-1 and ssIso-2, have less effect on RNA duplex thermal and serum stabilities, and their functional activities are also comparable to their native siRNAs. In contrast, antisense strand modifications with aminoisonucleoside at the corresponding positions, such as asIso-2 or asIso-1, bring a striking negative effect on RNA duplex stability but still maintain around 40-50% of gene knockdown.
引用
收藏
页码:1017 / 1024
页数:8
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