Aviñó Anna, Ocampo Sandra M, Perales José Carlos, Eritja Ramon
Institute for Research in Biomedicine (IRB Barcelona), Institute of Advanced Chemistry of Catalonia (IQAC-CSIC), Networking Centre on Bioengineering, Biomaterials, and Nanomedicine (CIBER-BBN), Baldiri Reixac 10, 08028 Barcelona, Spain.
J Nucleic Acids. 2011 Mar 6;2011:586935. doi: 10.4061/2011/586935.
Branched RNAs with two and four strands were synthesized. These structures were used to obtain branched siRNA. The branched siRNA duplexes had similar inhibitory capacity as those of unmodified siRNA duplexes, as deduced from gene silencing experiments of the TNF-α protein. Branched RNAs are considered novel structures for siRNA technology, and they provide an innovative tool for specific gene inhibition. As the method described here is compatible with most RNA modifications described to date, these compounds may be further functionalized to obtain more potent siRNA derivatives and can be attached to suitable delivery systems.
合成了具有两条和四条链的分支RNA。这些结构被用于获得分支小干扰RNA(siRNA)。从肿瘤坏死因子-α(TNF-α)蛋白的基因沉默实验推断,分支siRNA双链体具有与未修饰的siRNA双链体相似的抑制能力。分支RNA被认为是siRNA技术的新型结构,并且它们为特异性基因抑制提供了一种创新工具。由于此处描述的方法与迄今为止描述的大多数RNA修饰兼容,这些化合物可以进一步功能化以获得更有效的siRNA衍生物,并且可以连接到合适的递送系统上。