Scalable, methanol‐free manufacturing of the SARS‐CoV‐2 receptor‐binding domain in engineered Komagataella phaffii
Year: 2021
Type: article
Abstract: Prevention of COVID-19 on a global scale will require the continued development of high-volume, low-cost platforms for the manufacturing of vaccines to supply ongoing demand. Vaccine candidates based on recombinant protein subunits remain important because they can be manufactured at low costs in existing large-scale production facilities that use microbial hosts like Komagataella phaffii (Pichia pastoris). Here, we report an improved and scalable manufacturing approach for the SARS-CoV-2 spike protein receptor-binding domain (RBD); this protein is a key antigen for several reported vaccine candidates. We genetically engineered a manufacturing strain of K. phaffii to obviate the requirement for methanol induction of the recombinant gene. Methanol-free production improved the secreted titer of the RBD protein by >5X by alleviating protein folding stress. Removal of methanol from the production process enabled to scale up to a 1200 L pre-existing production facility. This engineered strain is now used to produce an RBD-based vaccine antigen that is currently in clinical trials and could be used to produce other variants of RBD as needed for future vaccines.
Source: Biotechnology and Bioengineering
DOI: 10.1002/bit.27979
Language: English
Subfield: Molecular Biology
Domain: Life Sciences
Open Access status: hybrid
Estimated APC paid: $4,600
Awards: G2360436881, G2507465183, Massachusetts Institute of Technology - To lower cost and increase feasibility for production of recombinant subunit vaccines., G5735053113, Beth Israel Deaconess Medical Center Inc. - to establish animal models for COVID-19 infection, to define the pathogenesis and immunology of infection, and to utilize these models to test vacc..., Cancer Center Support (Core) Grant
OpenAlex ID: W3213028588
