Bramsen Jesper B, Kjems Jørgen
Department of Molecular Biology, Interdisciplinary Nanoscience Center (iNANO), University of Aarhus, Aarhus, Denmark.
Methods Mol Biol. 2011;721:77-103. doi: 10.1007/978-1-61779-037-9_5.
Chemically synthesized siRNAs are widely used for gene silencing. For in vitro applications, stability, delivery, and immunological issues are rarely problematic, but for in vivo applications the situation is different. Limited stability, undesirable pharmacokinetic behaviour, and unanticipated side effects from the immune system call for more careful structural siRNA design and inclusion of chemical modifications at selected positions. Also the notion that siRNA induces significant off-target silencing of many non-related genes has promted new effective measures to enhance specificity. The scope of this review is to provide a simple guide to successful chemical and structural modification of siRNAs with improved activity, stability, specificity, and low toxicity.
化学合成的小干扰RNA(siRNA)被广泛用于基因沉默。对于体外应用,稳定性、递送和免疫问题很少成为难题,但对于体内应用,情况则有所不同。稳定性有限、不良的药代动力学行为以及免疫系统产生的意外副作用要求更谨慎地设计siRNA结构,并在选定位置引入化学修饰。此外,siRNA会诱导许多非相关基因产生显著的脱靶沉默这一观点也促使人们采取新的有效措施来提高特异性。本综述的目的是提供一个简单指南,指导如何成功地对siRNA进行化学和结构修饰,以提高其活性、稳定性、特异性并降低毒性。