Accessible Type 2 diabetes medication through stable expression of Exendin-4 in Saccharomyces cerevisiae
Diabetes mellitus affects roughly one in ten people globally and is the world's ninth leading cause of death. However, a significant portion of chronic complications that contribute to mortality can be prevented with proper treatment and medication. Glucagon-like peptide 1 receptor agonists, such as Exendin-4, are one of the leading classes of Type 2 diabetes treatments but are prohibitively expensive. In this study, experimental models for recombinant Exendin-4 protein production were designed in both <i>Escherichia coli</i> and <i>Saccharomyces cerevisiae</i>. Protein expression in the chromosomally integrated <i>S. cerevisiae</i> strain was observed at the expected size of Exendin-4 and confirmed by immunoassay. This provides a foundation for the use of this Generally Regarded as Safe organism as an affordable treatment for Type 2 diabetes that can be propagated, prepared, and distributed locally.
Authors
- Joanne X. Shen (ORCID: https://orcid.org/0009-0008-0322-5615)
- David L. Bernick (ORCID: https://orcid.org/0000-0003-1056-307X)
- L. Paule
- Gia Balius
- Jonathan Zau
- Zoë Petroff
- Thiago Brasileiro Feitosa
- C. VIBEKE STRAND
- Nathan Mccall
- N. Peng
- E. L. de Beer
- Vidhata Singh
- Kiana Imani
Institutions
- University of California, Santa Cruz (US)
Publication Details
- Journal
- Frontiers in Systems Biology
- Published
- 2024-09-02
- DOI
- https://doi.org/10.3389/fsysb.2024.1283371
- Primary Topic
- Diabetes Treatment and Management
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Directorate for Biological Sciences