Journal
COMPUTATIONAL AND STRUCTURAL BIOTECHNOLOGY JOURNAL
Volume 14, Issue -, Pages 404-410Publisher
ELSEVIER SCIENCE BV
DOI: 10.1016/j.csbj.2016.10.004
Keywords
Cell factory; Recombinant protein; Protein translation; Signal peptide; lncRNA; SINEUP
Funding
- Compagnia di San Paolo PhD scholarship
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Mammalian cells are an indispensable tool for the production of recombinant proteins in contexts where function depends on post-translational modifications. Among them, Chinese Hamster Ovary (CHO) cells are the primary factories for the production of therapeutic proteins, including monoclonal antibodies (MAbs). To improve expression and stability, several methodologies have been adopted, including methods based on media formulation, selective pressure and cell-or vector engineering. This review presents current approaches aimed at improving mammalian cell factories that are based on the enhancement of translation. Among well-established techniques (codon optimization and improvement of mRNA secondary structure), we describe SINEUPs, a family of antisense long non-coding RNAs that are able to increase translation of partially overlapping protein-coding mRNAs. By exploiting their modular structure, SINEUP molecules can be designed to target virtually any mRNA of interest, and thus to increase the production of secreted proteins. Thus, synthetic SINEUPs represent a new versatile tool to improve the production of secreted proteins in biomanufacturing processes. (C) 2016 The Authors. Published by Elsevier B.V. on behalf of Research Network of Computational and Structural Biotechnology.
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