Cargando…
High-throughput identification of peptide agonists against GPCRs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics
Since G-protein coupled receptors (GPCRs) are linked to various diseases, screening of functional ligands against GPCRs is vital for drug discovery. In the present study, we developed a high-throughput functional cell-based assay by combining human culture cells producing a GPCR, yeast cells secreti...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662714/ https://www.ncbi.nlm.nih.gov/pubmed/31358824 http://dx.doi.org/10.1038/s41598-019-47388-x |
_version_ | 1783439697058463744 |
---|---|
author | Yaginuma, Kenshi Aoki, Wataru Miura, Natsuko Ohtani, Yuta Aburaya, Shunsuke Kogawa, Masato Nishikawa, Yohei Hosokawa, Masahito Takeyama, Haruko Ueda, Mitsuyoshi |
author_facet | Yaginuma, Kenshi Aoki, Wataru Miura, Natsuko Ohtani, Yuta Aburaya, Shunsuke Kogawa, Masato Nishikawa, Yohei Hosokawa, Masahito Takeyama, Haruko Ueda, Mitsuyoshi |
author_sort | Yaginuma, Kenshi |
collection | PubMed |
description | Since G-protein coupled receptors (GPCRs) are linked to various diseases, screening of functional ligands against GPCRs is vital for drug discovery. In the present study, we developed a high-throughput functional cell-based assay by combining human culture cells producing a GPCR, yeast cells secreting randomized peptide ligands, and a droplet microfluidic device. We constructed a reporter human cell line that emits fluorescence in response to the activation of human glucagon-like peptide-1 receptor (hGLP1R). We then constructed a yeast library secreting an agonist of hGLP1R or randomized peptide ligands. We demonstrated that high-throughput identification of functional ligands against hGLP1R could be performed by co-culturing the reporter cells and the yeast cells in droplets. We identified functional ligands, one of which had higher activity than that of an original sequence. The result suggests that our system could facilitate the discovery of functional peptide ligands of GPCRs. |
format | Online Article Text |
id | pubmed-6662714 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-66627142019-08-02 High-throughput identification of peptide agonists against GPCRs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics Yaginuma, Kenshi Aoki, Wataru Miura, Natsuko Ohtani, Yuta Aburaya, Shunsuke Kogawa, Masato Nishikawa, Yohei Hosokawa, Masahito Takeyama, Haruko Ueda, Mitsuyoshi Sci Rep Article Since G-protein coupled receptors (GPCRs) are linked to various diseases, screening of functional ligands against GPCRs is vital for drug discovery. In the present study, we developed a high-throughput functional cell-based assay by combining human culture cells producing a GPCR, yeast cells secreting randomized peptide ligands, and a droplet microfluidic device. We constructed a reporter human cell line that emits fluorescence in response to the activation of human glucagon-like peptide-1 receptor (hGLP1R). We then constructed a yeast library secreting an agonist of hGLP1R or randomized peptide ligands. We demonstrated that high-throughput identification of functional ligands against hGLP1R could be performed by co-culturing the reporter cells and the yeast cells in droplets. We identified functional ligands, one of which had higher activity than that of an original sequence. The result suggests that our system could facilitate the discovery of functional peptide ligands of GPCRs. Nature Publishing Group UK 2019-07-29 /pmc/articles/PMC6662714/ /pubmed/31358824 http://dx.doi.org/10.1038/s41598-019-47388-x Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yaginuma, Kenshi Aoki, Wataru Miura, Natsuko Ohtani, Yuta Aburaya, Shunsuke Kogawa, Masato Nishikawa, Yohei Hosokawa, Masahito Takeyama, Haruko Ueda, Mitsuyoshi High-throughput identification of peptide agonists against GPCRs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics |
title | High-throughput identification of peptide agonists against GPCRs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics |
title_full | High-throughput identification of peptide agonists against GPCRs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics |
title_fullStr | High-throughput identification of peptide agonists against GPCRs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics |
title_full_unstemmed | High-throughput identification of peptide agonists against GPCRs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics |
title_short | High-throughput identification of peptide agonists against GPCRs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics |
title_sort | high-throughput identification of peptide agonists against gpcrs by co-culture of mammalian reporter cells and peptide-secreting yeast cells using droplet microfluidics |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6662714/ https://www.ncbi.nlm.nih.gov/pubmed/31358824 http://dx.doi.org/10.1038/s41598-019-47388-x |
work_keys_str_mv | AT yaginumakenshi highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT aokiwataru highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT miuranatsuko highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT ohtaniyuta highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT aburayashunsuke highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT kogawamasato highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT nishikawayohei highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT hosokawamasahito highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT takeyamaharuko highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics AT uedamitsuyoshi highthroughputidentificationofpeptideagonistsagainstgpcrsbycocultureofmammalianreportercellsandpeptidesecretingyeastcellsusingdropletmicrofluidics |