Study on the Characterization and Degradation Pattern of Circular RNA Vaccines Using an HPLC Method

降级(电信) 高效液相色谱法 环状RNA 计算生物学 核糖核酸 化学 免疫原性 色谱法 生物 生物化学 计算机科学 遗传学 基因 抗原 电信
作者
Feiran Cheng,Ji Li,Chaoying Hu,Yu Bai,Jianyang Liu,Dong Liu,Qian He,Qiuheng Jin,Qunying Mao,Zhenglun Liang,Miao Xu
出处
期刊:Chemosensors [Multidisciplinary Digital Publishing Institute]
卷期号:12 (7): 120-120 被引量:17
标识
DOI:10.3390/chemosensors12070120
摘要

Circular RNA (circRNA) vaccines have attracted increasing attention due to their stable closed-loop structures and persistent protein expression ability. During the synthesis process, nicked circRNAs with similar molecular weights to those of circRNAs are generated. Analytical techniques based on differences in molecular weight, such as capillary electrophoresis, struggle to distinguish between circRNAs and nicked circRNAs. The characteristic degradation products of circRNAs and their biological activities remain unclear. Therefore, developing methods to identify target circRNAs and non-target components and investigating degradation patterns will be beneficial to gaining an in-depth understanding of the properties and quality control of circRNAs vaccines. The reversed-phase HPLC (RP-HPLC) method was established for identification of target circRNAs, product-related substances, and impurities. Subsequently, we investigated the degradation patterns of circRNAs under thermal acceleration conditions and performed biological analysis of degradation products and linear precursors. Here, RP-HPLC method effectively identified circRNAs and nicked circRNAs. With thermal acceleration, circRNAs exhibited a “circular→nicked circRNAs→degradation products” degradation pattern. Biological analysis revealed that the immunogenicity of degradation products significantly decreased, whereas linear precursors did not possess immunogenicity. Thus, our established RP-HPLC method can be used for purity analysis of circRNA vaccines, which contributes to the quality control of circRNA vaccines and promoting the development of circRNA technology.
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