Molecular engineering improves antigen quality and enables integrated manufacturing of a trivalent subunit vaccine candidate for rotavirus

• Published in: Microbial cell factories 2021-05, Vol.20 (1), p.94-94, Article 94
• Main Authors: Dalvie, Neil C, Brady, Joseph R, Crowell, Laura E, Tracey, Mary Kate, Biedermann, Andrew M, Kaur, Kawaljit, Hickey, John M, Kristensen, 2nd, D Lee, Bonnyman, Alexandra D, Rodriguez-Aponte, Sergio A, Whittaker, Charles A, Bok, Marina, Vega, Celina, Mukhopadhyay, Tarit K, Joshi, Sangeeta B, Volkin, David B, Parreño, Viviana, Love, Kerry R, Love, J Christopher
• Format: Article
• Language: English
• Subjects: Amino acids; Antigenicity; Antigens; Biochemical engineering; Biomanufacturing; Chromatography; Continuous production; Design; E coli; Engineering; Genetic engineering; Immunogenicity; Manufacturability; Manufacturing; Manufacturing industry; Methods; Molecular weight; Nucleotide sequence; Perfusion; Pharmaceutical research; Pichia pastoris; Prevention; Production processes; Productivity; Proteins; Quality by design; Recombinant proteins; Rotavirus; Rotavirus infections; Serotypes; Subunit vaccine; Tetanus; Vaccines; Viral vaccines; Viruses; Yeasts
• ISSN: 1475-2859; 1475-2859
• DOI: 10.1186/s12934-021-01583-6

Vaccines comprising recombinant subunit proteins are well-suited to low-cost and high-volume production for global use. The design of manufacturing processes to produce subunit vaccines depends, however, on the inherent biophysical traits presented by an individual antigen of interest. New candidate antigens typically require developing custom processes for each one and may require unique steps to ensure sufficient yields without product-related variants. We describe a holistic approach for the molecular design of recombinant protein antigens-considering both their manufacturability and antigenicity-informed by bioinformatic analyses such as RNA-seq, ribosome profiling, and sequence-based prediction tools. We demonstrate this approach by engineering the product sequences of a trivalent non-replicating rotavirus vaccine (NRRV) candidate to improve titers and mitigate product variants caused by N-terminal truncation, hypermannosylation, and aggregation. The three engineered NRRV antigens retained their original antigenicity and immunogenicity, while their improved manufacturability enabled concomitant production and purification of all three serotypes in a single, end-to-end perfusion-based process using the biotechnical yeast Komagataella phaffii. This study demonstrates that molecular engineering of subunit antigens using advanced genomic methods can facilitate their manufacturing in continuous production. Such capabilities have potential to lower the cost and volumetric requirements in manufacturing vaccines based on recombinant protein subunits.