Recombinant Ranpirnase enhances the expression of co-transfected mRNA by modulating cellular metabolic activity
Xiujin WuiD, Chen LiangiD, Yingxue Lei, Peng XuiD, Yaoyi ZhangiD, Guang YangiD, Hailin Yin, Kai XuiD
Abstract
As the worlds first approved prophylactic mRNA vaccine, the development of the Covid-19 mRNA vaccine marks a milestone in mRNA therapeutics. However, achieving efficient transgene expression in therapeutic applications such as protein replacement and cancer therapeutical vaccines remains challenging. This study explores the use of recombinant Ranpirnase, a small ribonuclease, as a novel expression-enhancing tool for mRNA-based therapeutics. In Balb/c mice, co-expression of Ranpirnase significantly increased transgene expression levels by 3-to 6-fold and prolonged expression duration by more than 85%, regardless of mRNA nucleoside modification status. Recombinant Ranpirnase induces a cytostatic state in host cells, stabilizing mRNA and protein transcripts, thereby enhancing transgene expression. Importantly, co-expression of Ranpirnase recombinants did not cause detectable cytotoxicity or alter the tissue distribution of transgene expression, ensuring safety and tolerability at higher translation levels. The compact size of the recombinant Ranpirnase gene allows for seamless fusion with the target gene or co-transfection with existing delivery technologies. Altogether, recombinant Ranpirnase shows promise as an expression-enhancing element in mRNA-based therapeutics, including veterinary applications.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 0
- Organism
- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A flexible, efficient, and scalable platform to produce circular RNAs as new therapeutics
- Efficient heterologous mRNA production in E. coli via protein-facilitated protection
Zongsheng Zou, Tayyaba Younas, … Lizhong He·bioRxiv·Jun 16, 2026
- Combinatorial optimization of mRNA structure, stability, and translation for RNA-based therapeutics
Kathrin Leppek, Gun Woo Byeon, … Rhiju Das·Nature CommunicationsPeer-reviewed·Mar 22, 2022
- Improving mRNA vaccine safety and efficiency with cationized lipid nanoparticle formula
Peng Xu, Guangneng Liao, … Kai Xu·bioRxiv·Mar 29, 2023
- Optimization of mRNA Synthesis and its Cell Expression for Vaccine Development
Subrata Kumar Das, Gaurav Dutt, … A. B. Joshi·bioRxiv·May 13, 2025
- Highly efficient cellular expression of circular mRNA enables prolonged protein expression
Mildred J. Unti, Samie R. Jaffrey·Cell chemical biologyPeer-reviewed·Oct 25, 2023