Gia Balius, Kiana Imani, Zoë Petroff, Elizabeth Beer, Thiago Brasileiro Feitosa, Nathan Mccall, Lauren Paule, Neo Yixuan Peng, Joanne Shen, Vidhata Singh, Cambell Strand, Jonathan Zau, D L Bernick
{"title":"通过酿酒酵母中Exendin-4的稳定表达可获得2型糖尿病药物。","authors":"Gia Balius, Kiana Imani, Zoë Petroff, Elizabeth Beer, Thiago Brasileiro Feitosa, Nathan Mccall, Lauren Paule, Neo Yixuan Peng, Joanne Shen, Vidhata Singh, Cambell Strand, Jonathan Zau, D L Bernick","doi":"10.3389/fsysb.2024.1283371","DOIUrl":null,"url":null,"abstract":"<p><p>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.</p>","PeriodicalId":73109,"journal":{"name":"Frontiers in systems biology","volume":"4 ","pages":"1283371"},"PeriodicalIF":2.3000,"publicationDate":"2024-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342014/pdf/","citationCount":"0","resultStr":"{\"title\":\"Accessible Type 2 diabetes medication through stable expression of Exendin-4 in <i>Saccharomyces cerevisiae</i>.\",\"authors\":\"Gia Balius, Kiana Imani, Zoë Petroff, Elizabeth Beer, Thiago Brasileiro Feitosa, Nathan Mccall, Lauren Paule, Neo Yixuan Peng, Joanne Shen, Vidhata Singh, Cambell Strand, Jonathan Zau, D L Bernick\",\"doi\":\"10.3389/fsysb.2024.1283371\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>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.</p>\",\"PeriodicalId\":73109,\"journal\":{\"name\":\"Frontiers in systems biology\",\"volume\":\"4 \",\"pages\":\"1283371\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2024-09-02\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12342014/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Frontiers in systems biology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.3389/fsysb.2024.1283371\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in systems biology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/fsysb.2024.1283371","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/1/1 0:00:00","PubModel":"eCollection","JCR":"","JCRName":"","Score":null,"Total":0}
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 Escherichia coli and Saccharomyces cerevisiae. Protein expression in the chromosomally integrated S. cerevisiae 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.