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New Screening Assay for Finding Ghrelin Receptor Drug Candidates

evidence
The takeaway

A homogeneous time-resolved fluorescence assay was developed for high-throughput screening of GHS-R1a ligands, enabling rapid identification of novel ghrelin receptor drug candidates for obesity and GH deficiency.

Key finding

A homogeneous time-resolved fluorescence assay was developed for high-throughput screening of GHS-R1a ligands, enabling rapid identification of novel

What the researchers found

A homogeneous time-resolved fluorescence assay was developed for high-throughput screening of GHS-R1a ligands, enabling rapid identification of novel ghrelin receptor drug candidates for obesity and GH deficiency.

Why it matters

Relevant for peptide research.

How the study worked

research study.

What this study cannot tell us

See abstract.

How to read the evidence

emerging evidence.

When this study was published

Published in 2011.

The bigger picture

Advances peptide research.

Questions still open

  • Further research needed.

Common questions

What was studied?
New Screening Assay for Finding Ghrelin Receptor Drug Candidates
What was found?
A homogeneous time-resolved fluorescence assay was developed for high-throughput screening of GHS-R1a ligands, enabling rapid identification of novel ghrelin receptor drug candidates for obesity and GH deficiency.

Read the original research

Homogeneous time-resolved fluorescence-based assay to screen for ligands targeting the growth hormone secretagogue receptor type 1a.

Analytical biochemistry, 408(2), 253-62

Citation

Leyris, Jean-Philippe; Roux, Thomas; Trinquet, Eric; Verdié, Pascal; Fehrentz, Jean-Alain; Oueslati, Nadia; Douzon, Stéphanie; Bourrier, Emmanuel; Lamarque, Laurent; Gagne, Didier; Galleyrand, Jean-Claude; M'kadmi, Céline; Martinez, Jean; Mary, Sophie; Banères, Jean-Louis; Marie, Jacky. (2011). Homogeneous time-resolved fluorescence-based assay to screen for ligands targeting the growth hormone secretagogue receptor type 1a.. Analytical biochemistry, 408(2), 253-62. https://doi.org/10.1016/j.ab.2010.09.030