{"title":"Production and purification of recombinant long protein isoforms of FGF11 subfamily","authors":"Martyna Biadun , Szymon Sidor , Marta Kalka , Radoslaw Karelus , Martyna Sochacka , Daniel Krowarsch , Lukasz Opalinski , Malgorzata Zakrzewska","doi":"10.1016/j.jbiotec.2025.03.016","DOIUrl":null,"url":null,"abstract":"<div><div>The FGF11 subfamily of FGF proteins also known as fibroblast growth factor homologous factors (FHFs) includes four proteins, FGF11, FGF12, FGF13, and FGF14. They are mainly expressed in excitable cells but are also present in fibroblasts or osteoclasts, where their function is much less understood. Each FGF11–14 protein has at least two isoforms formed by alternative splicing, which differ in both cellular localization and function. Until recently, only the short isoforms had been efficiently produced and purified in recombinant form. Here, we developed a protocol to produce in the bacterial expression system and efficiently purify the long “a” isoforms of FGF11, FGF12, FGF13 and FGF14. In addition, we characterized their biophysical and biological properties, demonstrating that they activate downstream signaling and, unlike short “b” isoforms, induce cell proliferation.</div></div>","PeriodicalId":15153,"journal":{"name":"Journal of biotechnology","volume":"403 ","pages":"Pages 9-16"},"PeriodicalIF":4.1000,"publicationDate":"2025-03-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of biotechnology","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0168165625000744","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
Abstract
The FGF11 subfamily of FGF proteins also known as fibroblast growth factor homologous factors (FHFs) includes four proteins, FGF11, FGF12, FGF13, and FGF14. They are mainly expressed in excitable cells but are also present in fibroblasts or osteoclasts, where their function is much less understood. Each FGF11–14 protein has at least two isoforms formed by alternative splicing, which differ in both cellular localization and function. Until recently, only the short isoforms had been efficiently produced and purified in recombinant form. Here, we developed a protocol to produce in the bacterial expression system and efficiently purify the long “a” isoforms of FGF11, FGF12, FGF13 and FGF14. In addition, we characterized their biophysical and biological properties, demonstrating that they activate downstream signaling and, unlike short “b” isoforms, induce cell proliferation.
期刊介绍:
The Journal of Biotechnology has an open access mirror journal, the Journal of Biotechnology: X, sharing the same aims and scope, editorial team, submission system and rigorous peer review.
The Journal provides a medium for the rapid publication of both full-length articles and short communications on novel and innovative aspects of biotechnology. The Journal will accept papers ranging from genetic or molecular biological positions to those covering biochemical, chemical or bioprocess engineering aspects as well as computer application of new software concepts, provided that in each case the material is directly relevant to biotechnological systems. Papers presenting information of a multidisciplinary nature that would not be suitable for publication in a journal devoted to a single discipline, are particularly welcome.