Lee Li Kim, Dunham Brandee M, Li Zhuting, Roth Charles M
Department of Chemical and Biochemical Engineering, Rutgers University, Piscataway, NJ 08854-8058, USA.
Ann N Y Acad Sci. 2006 Oct;1082:47-51. doi: 10.1196/annals.1348.061.
We aim to compare quantitatively the dynamics of the effectiveness of antisense oligonucleotides (AS ODNs) versus short interfering RNAs (siRNAs) and relate their effectiveness to sequence metrics (e.g., predicted free energy of binding). AS ODNs against a quantitative model target, pd1EGFP (destabilized enhanced GFP [green fluorescent protein]), were selected using our thermodynamic model, and siRNA sequences were designed to be identical to the AS ODN sequences in the antisense strand. We evaluated d1EGFP inhibition in transiently and stably transfected Chinese hamster ovary (CHO) cells over time using flow cytometry. Overall, our results show that the rationally designed AS ODN and siRNA sequences proved effective inhibitors of GFP expression and suggest that certain regions of mRNA may be susceptible to both AS ODNs and siRNAs.
我们旨在定量比较反义寡核苷酸(AS ODNs)与小干扰RNA(siRNAs)的有效性动态,并将它们的有效性与序列指标(例如预测的结合自由能)相关联。使用我们的热力学模型选择针对定量模型靶标pd1EGFP(不稳定增强型绿色荧光蛋白[GFP])的AS ODNs,并将siRNA序列设计为与反义链中的AS ODN序列相同。我们使用流式细胞术评估了随时间推移在瞬时和稳定转染的中国仓鼠卵巢(CHO)细胞中d1EGFP的抑制情况。总体而言,我们的结果表明,合理设计的AS ODN和siRNA序列被证明是GFP表达的有效抑制剂,并表明mRNA的某些区域可能对AS ODNs和siRNAs均敏感。