Abstract

G‐protein coupled receptors (GPCRs) which feature a seven‐transmembrane structure are involved in various diseases as well as in regulating physiological functions. Phage display has been used for discovering bioactive peptides, but the methodology is never effective for screening GPCR‐agonists because phage‐displayed peptides are screened based only on binding ability and are different from their final soluble form. In this study, we established a functional screening system for GPCR‐activating peptides by combining peptide‐secreting yeasts with GPCRs‐producing mammalian cells. Glucagon‐like peptide‐1 receptor (GLP1R) and its peptide agonist exendin‐4 (Ex4) were used as model molecules. Ex4‐secreting yeast (Ex4‐yeast) was constructed by introducing the Ex4‐encoding gene linked to secretion signal genes of glucoamylase or yeast α‐factor into Saccharomyces cerevisiae. Detection of yeast‐secreted Ex4 was performed by evaluating cAMP production in GLP1R‐producing CHO cells exposed to yeast culture medium incubated in glass tube and microplate. Model screening of Ex4‐yeast from mixture containing Ex4‐ and control‐yeasts (ratio of each cell number, 1:9) was carried out on microplate. The results indicated that the functional screening system with peptide‐secreting yeasts would be promising for efficient discovery of novel peptide‐based GPCR agonists [1]. [1] Shigemori et al. submitted.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.