Scalable Cell-Free Production of Active T7 RNA Polymerase
- PMID: 40296704
- DOI: 10.1002/bit.28993
Scalable Cell-Free Production of Active T7 RNA Polymerase
Abstract
The SARS-CoV-2 pandemic highlighted the urgent need for biomanufacturing paradigms that are robust and fast. Here, we demonstrate the rapid process development and scalable cell-free production of T7 RNA polymerase, a critical component in mRNA vaccine synthesis. We carry out a 1-L cell-free gene expression (CFE) reaction that achieves over 90% purity, low endotoxin levels, and enhanced activity relative to commercial T7 RNA polymerase. To achieve this demonstration, we implement rolling circle amplification to circumvent difficulties in DNA template generation, and tune cell-free reaction conditions, such as temperature, additives, purification tags, and agitation, to boost yields. We achieve production of a similar quality and titer of T7 RNA polymerase over more than four orders of magnitude in reaction volume. This proof of principle positions CFE as a viable solution for decentralized biotherapeutic manufacturing, enhancing preparedness for future public health crises or emergent threats.
Keywords: T7 RNA polymerase; biomanufacturing; cell‐free gene expression; in vitro transcription and translation; protein synthesis; scale‐up.
© 2025 Wiley Periodicals LLC.
References
-
- Adiga, R., M. Al‐Adhami, A. Andar, et al. 2018. “Point‐of‐Care Production of Therapeutic Proteins of Good‐Manufacturing‐Practice Quality.” Nature Biomedical Engineering 2, no. 9: 675–686. https://doi.org/10.1038/s41551-018-0259-1.
-
- Bolgiano, B., F. Mawas, K. Burkin, et al. 2007. “A Retrospective Study on the Quality of Haemophilus Influenzae Type B Vaccines Used in the UK Between 1996 and 2004.” Human Vaccines 3, no. 5: 176–182. https://doi.org/10.4161/hv.3.5.4352.
-
- Borhani, S. G., M. Z. Levine, L. H. Krumpe, et al. 2023. “An Approach to Rapid Distributed Manufacturing of Broad Spectrum Anti‐Viral Griffithsin Using Cell‐Free Systems to Mitigate Pandemics.” New Biotechnology 76: 13–22. https://doi.org/10.1016/j.nbt.2023.04.003.
-
- Brito, L. A., and M. Singh. 2011. “Commentary: Acceptable Levels of Endotoxin in Vaccine Formulations During Preclinical Research.” Journal of Pharmaceutical Sciences 100, no. 1: 34–37. https://doi.org/10.1002/jps.22267.
-
- Bundy, B. C., J. P. Hunt, M. C. Jewett, et al. 2018. “Cell‐Free Biomanufacturing.” Current Opinion in Chemical Engineering 22: 177–183. https://doi.org/10.1016/j.coche.2018.10.003.
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Miscellaneous
