Evidence map›Paper›PMID 39824656›Full record

ArticleFEMS yeast research2025

Development of a yeast-based sensor platform for evaluation of ligands recognized by the human free fatty acid 2 receptor.

Andrea Clausen Lind, Davi De Castro Gomes, Ricardo Bisquert, Jonas Mårtensson, Martina Sundqvist, Huamei Forsman, Claes Dahlgren, Florian David, Verena Siewers

Abstract read
In one paragraph

Article in FEMS yeast research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Andrea Clausen LindDepartment of Life Sciences, Chalmers University of Technology, 412 96 Gothenburg, Sweden.ORCID 0009-0006-7117-3496
Davi De Castro GomesDepartment of Genetics, Evolution, Microbiology and Immunology, Institute of Biology, University of Campinas, 13083-862 Campinas, São Paulo, Brazil.
Ricardo BisquertDepartment of Life Sciences, Chalmers University of Technology, 412 96 Gothenburg, Sweden.ORCID 0000-0001-6381-8852
Jonas MårtenssonDepartment of Rheumatology and Inflammation Research, Institute of Medicine, The Sahlgrenska Academy, University of Gothenburg, 413 90 Gothenburg, Sweden.
Martina SundqvistDepartment of Rheumatology and Inflammation Research, Institute of Medicine, The Sahlgrenska Academy, University of Gothenburg, 413 90 Gothenburg, Sweden.
Huamei ForsmanDepartment of Rheumatology and Inflammation Research, Institute of Medicine, The Sahlgrenska Academy, University of Gothenburg, 413 90 Gothenburg, Sweden.
Claes DahlgrenDepartment of Rheumatology and Inflammation Research, Institute of Medicine, The Sahlgrenska Academy, University of Gothenburg, 413 90 Gothenburg, Sweden.ORCID 0000-0002-8946-5714
Florian DavidDepartment of Life Sciences, Chalmers University of Technology, 412 96 Gothenburg, Sweden.
Verena SiewersDepartment of Life Sciences, Chalmers University of Technology, 412 96 Gothenburg, Sweden.

Funding

CAPESChalmers University of Technology 88887.687701/2022-00Joint Programming Initiative on Antimicrobial ResistanceNovo Nordisk Foundation NNF10CC1016517STINTSwedish Research Council 2019-00304
6 · The paper itself

Abstract

Yeast-based sensors have shown great applicability for deorphanization of G protein-coupled receptors (GPCRs) and screening of ligands targeting these. A GPCR of great interest is free fatty acid 2 receptor (FFA2R), for which short-chain fatty acids such as propionate and acetate are agonists. FFA2R regulates a wide array of downstream receptor signaling pathways in both adipose tissue and immune cells and has been recognized as a promising therapeutic target, having been implicated in several metabolic and inflammatory diseases. While research aiming to identify ligands recognized by FFA2R for translational applications is ongoing, screening is complicated by the complex regulatory and cell-specific responses mediated by the receptor. To simplify screening towards identification of novel ligands, heterologous platforms are valuable tools that offer efficient identification of ligand activity in the absence of regulatory mechanisms. Here, we present a yeast-based sensor designed to evaluate G protein α i1-mediated FFA2R signaling, with an assay time of 3 h. We verify this platform towards the natural agonists, propionate and acetate, and show applicability towards evaluation of synthetic agonists, antagonists, and allosteric agonists. As such, we believe that the developed yeast strain constitutes a promising screening platform for effective evaluation of ligands acting on FFA2R.

Indexed as

Biosensing TechniquesReceptors, G-Protein-CoupledSaccharomyces cerevisiaeAcetatesHumansLigandsPropionatesSignal TransductionAcetatesFFAR2 protein, humanLigandsPropionatesReceptors, G-Protein-CoupledbiosensorsFFAR2GPCRGPR43ligand screeningyeast mating pathway

Identifiers

PMID39824656
PMCPMC11781196

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.