Department of Energy, Environmental & Chemical Engineering, Washington University in St. Louis, St. Louis, Missouri 63130, United States.
Environ Sci Technol. 2021 Jun 15;55(12):8045-8053. doi: 10.1021/acs.est.1c01255. Epub 2021 May 25.
Phosphodiester bonds in the backbones of double-stranded (ds)RNA and single-stranded (ss)RNA are known to undergo alkaline hydrolysis. Consequently, dsRNA agents used in emerging RNA interference (RNAi) products have been assumed to exhibit low chemical persistence in solutions. However, the impact of the duplex structure of dsRNA on alkaline hydrolysis has not yet been evaluated. In this study, we demonstrated that dsRNA undergoes orders-of-magnitude slower alkaline hydrolysis than ssRNA. Furthermore, we observed that dsRNA remains intact for multiple months at neutral pH, challenging the assumption that dsRNA is chemically unstable. In systems enabling both enzymatic degradation and alkaline hydrolysis of dsRNA, we found that increasing pH effectively attenuated enzymatic degradation without inducing alkaline hydrolysis that was observed for ssRNA. Overall, our findings demonstrated, for the first time, that key degradation pathways of dsRNA significantly differ from those of ssRNA. Consideration of the unique properties of dsRNA will enable greater control of dsRNA stability during the application of emerging RNAi technology and more accurate assessment of its fate in environmental and biological systems, as well as provide insights into broader application areas including dsRNA isolation, detection and inactivation of dsRNA viruses, and prebiotic molecular evolution.
双链 (ds)RNA 和单链 (ss)RNA 骨架中的磷酸二酯键已知会发生碱性水解。因此,新兴 RNA 干扰 (RNAi) 产品中使用的 dsRNA 制剂被认为在溶液中具有低化学稳定性。然而,dsRNA 双螺旋结构对碱性水解的影响尚未得到评估。在这项研究中,我们证明 dsRNA 的碱性水解速度比 ssRNA 慢几个数量级。此外,我们观察到 dsRNA 在中性 pH 下能保持完整数月,这挑战了 dsRNA 在化学上不稳定的假设。在允许 dsRNA 酶降解和碱性水解的系统中,我们发现增加 pH 可有效抑制酶降解,而不会诱导 ssRNA 发生的碱性水解。总的来说,我们的研究结果首次表明,dsRNA 的关键降解途径与其 ssRNA 显著不同。考虑到 dsRNA 的独特性质,将能够在新兴的 RNAi 技术应用中更好地控制 dsRNA 的稳定性,并更准确地评估其在环境和生物系统中的命运,以及为更广泛的应用领域提供深入了解,包括 dsRNA 的分离、dsRNA 病毒的检测和失活,以及前生物分子进化。