» Articles » PMID: 34752330

Evaluating Functional Ligand-GPCR Interactions in Cell-based Assays

Overview
Specialty Cell Biology
Date 2021 Nov 9
PMID 34752330
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

G protein-coupled receptors (GPCRs) are a family of transmembrane proteins that act as major mediators of cellular signaling, and are the primary targets for a large portion of clinical therapeutics. Despite their critical role in biology and medicine, a large number of GPCRs are poorly understood, lacking validated ligands or potent synthetic modulators. Ligand-induced GPCR activation can be measured in cell-based assays to test hypotheses about ligand-receptor interactions or to evaluate efficacy of synthetic agonists or antagonists. However, the techniques necessary to develop and implement a cell-based assay to study a given receptor of interest are not commonplace in all laboratories. This chapter outlines methods to develop a cell-based assay to evaluate agonist-induced activation for a GPCR of interest, which can be useful to evaluate the effectiveness of predicted ligands. Examples of sample preparation protocols and data analysis are provided to help researchers from interdisciplinary fields, especially those in fields with relatively little molecular biology or cell culture experience.

Citing Articles

Affinity-Driven Aryl Diazonium Labeling of Peptide Receptors on Living Cells.

Sharma S, Naldrett M, Gill M, Checco J J Am Chem Soc. 2024; 146(19):13676-13688.

PMID: 38693710 PMC: 11149697. DOI: 10.1021/jacs.4c04672.


Characterization of an vasotocin signaling system and actions of posttranslational modifications and individual residues of the ligand on receptor activity.

Xu J, Ding X, Guo S, Wang H, Liu W, Jiang H Front Pharmacol. 2023; 14:1132066.

PMID: 37021048 PMC: 10067623. DOI: 10.3389/fphar.2023.1132066.


Endogenous l- to d-amino acid residue isomerization modulates selectivity between distinct neuropeptide receptor family members.

Yussif B, Blasing C, Checco J Proc Natl Acad Sci U S A. 2023; 120(11):e2217604120.

PMID: 36877849 PMC: 10089201. DOI: 10.1073/pnas.2217604120.

References
1.
Kostenis E, Martini L, Ellis J, Waldhoer M, Heydorn A, Rosenkilde M . A highly conserved glycine within linker I and the extreme C terminus of G protein alpha subunits interact cooperatively in switching G protein-coupled receptor-to-effector specificity. J Pharmacol Exp Ther. 2004; 313(1):78-87. DOI: 10.1124/jpet.104.080424. View

2.
Checco J, Zhang G, Yuan W, Yu K, Yin S, Roberts-Galbraith R . Molecular and Physiological Characterization of a Receptor for d-Amino Acid-Containing Neuropeptides. ACS Chem Biol. 2018; 13(5):1343-1352. PMC: 5962930. DOI: 10.1021/acschembio.8b00167. View

3.
Fricker L, Devi L . Orphan neuropeptides and receptors: Novel therapeutic targets. Pharmacol Ther. 2017; 185:26-33. PMC: 5899030. DOI: 10.1016/j.pharmthera.2017.11.006. View

4.
Aiyar N, Rand K, Elshourbagy N, Zeng Z, Adamou J, Bergsma D . A cDNA encoding the calcitonin gene-related peptide type 1 receptor. J Biol Chem. 1996; 271(19):11325-9. DOI: 10.1074/jbc.271.19.11325. View

5.
Foster S, Hauser A, Vedel L, Strachan R, Huang X, Gavin A . Discovery of Human Signaling Systems: Pairing Peptides to G Protein-Coupled Receptors. Cell. 2019; 179(4):895-908.e21. PMC: 6838683. DOI: 10.1016/j.cell.2019.10.010. View