Application of the iPLUS non-coding sequence in improving biopharmaceuticals production

• Published in: Frontiers in bioengineering and biotechnology 2024-02, Vol.12, p.1355957-1355957
• Main Authors: Reis-Claro, Inês, Silva, Maria Inês, Moutinho, Ana, Garcia, Beatriz C, Pereira-Castro, Isabel, Moreira, Alexandra
• Format: Article
• Language: English
• Subjects: 3′UTR; Bioengineering and Biotechnology; cis-regulatory sequences; iPLUS; mRNA therapeutics; recombinant protein expression; USE
• ISSN: 2296-4185; 2296-4185
• DOI: 10.3389/fbioe.2024.1355957

The biotechnological landscape has witnessed significant growth in biological therapeutics particularly in the field of recombinant protein production. Here we investigate the function of 3'UTR -regulatory elements in increasing mRNA and protein levels in different biological therapeutics and model systems, spanning from monoclonal antibodies to mRNA vaccines. We explore the regulatory function of iPLUS - a universal sequence capable of consistently augmenting recombinant protein levels. By incorporating iPLUS in a vector to express a monoclonal antibody used in immunotherapy, in a mammalian cell line used by the industry (ExpiCHO), trastuzumab production increases by 2-fold. As yeast is widely used in the manufacture of industrial enzymes and pharmaceuticals, we then used iPLUS in tandem (3x) and iPLUSv2 (a variant of iPLUS) to provide proof-of-concept data that it increases the production of a reporter protein more than 100-fold. As iPLUS functions by also increasing mRNA levels, we hypothesize that these sequences could be used as an asset in the mRNA vaccine industry. In fact, by including iPLUSv2 downstream of Spike we were able to double its production. Moreover, the same effect was observed when we introduced iPLUSv2 downstream of MAGEC2, a tumor-specific antigen tested for cancer mRNA vaccines. Taken together, our study provides data (TLR4) showing that iPLUS may be used as a valuable asset in a variety of systems used by the biotech and biopharmaceutical industry. Our results underscore the critical role of non-coding sequences in controlling gene expression, offering a promising avenue to accelerate, enhance, and cost-effectively optimize biopharmaceutical production processes.