小干扰RNA
纳米医学
核酸
核糖核酸
纳米技术
掷骰子
RNA干扰
纳米颗粒
化学
材料科学
生物化学
基因
作者
Kirill A. Afonin,Wade W. Grabow,Faye Walker,Eckart Bindewald,Marina A. Dobrovolskaia,Bruce A. Shapiro,Luc Jaeger
出处
期刊:Nature Protocols
[Springer Nature]
日期:2011-12-01
卷期号:6 (12): 2022-2034
被引量:175
标识
DOI:10.1038/nprot.2011.418
摘要
Individual genes can be targeted with siRNAs. The use of nucleic acid nanoparticles (NPs) is a convenient method for delivering combinations of specific siRNAs in an organized and programmable manner. We present three assembly protocols to produce two different types of RNA self-assembling functional NPs using processes that are fully automatable. These NPs are engineered based on two complementary nanoscaffold designs (nanoring and nanocube), which serve as carriers of multiple siRNAs. The NPs are functionalized by the extension of up to six scaffold strands with siRNA duplexes. The assembly protocols yield functionalized RNA NPs, and we show that they interact in vitro with human recombinant Dicer to produce siRNAs. Our design strategies allow for fast, economical and easily controlled production of endotoxin-free therapeutic RNA NPs that are suitable for preclinical development.
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