Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

GPCRs modulate a plethora of physiological processes and mediate the effects of one-third of FDA-approved drugs. Depending on which ligand activates a receptor, it can engage different intracellular transducers. This 'biased signalling' paradigm requires that we now characterize physiological signalling not just by receptors but by ligand-receptor pairs. Ligands eliciting biased signalling may constitute better drugs with higher efficacy and fewer adverse effects. However, ligand bias is very complex, making reproducibility and description challenging. Here, we provide guidelines and terminology for any scientists to design and report ligand bias experiments. The guidelines will aid consistency and clarity, as the basic receptor research and drug discovery communities continue to advance our understanding and exploitation of ligand bias. Scientific insight, biosensors, and analytical methods are still evolving and should benefit from and contribute to the implementation of the guidelines, together improving translation from in vitro to disease-relevant in vivo models.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7612872PMC
http://dx.doi.org/10.1111/bph.15811DOI Listing

Publication Analysis

Top Keywords

ligand bias
16
ligand
5
community guidelines
4
guidelines gpcr
4
gpcr ligand
4
bias
4
bias iuphar
4
iuphar review
4
review gpcrs
4
gpcrs modulate
4

Similar Publications

Bidirectional Modification of a Alkaloid Identifies Selective Opioid Ligands.

ACS Cent Sci

August 2025

Department of Chemistry, Scripps Research, La Jolla, California 92037, United States.

We report a bidirectional diversification and optimization campaign of the newly identified - and -opioid receptor antagonist GB18, a naturally occurring alkaloid. First, we find that replacement of the GB18 piperidine with pyridine alters the pharmacology from antagonism to partial agonism, with reduced potency but markedly higher receptor selectivity for over . Second, we optimize this hit via development of a mutually chemoselective cross-coupling of an alkyl iodide/vinyl triflate pair that leads to a series of low- and sub-nanomolar KOR-selective full agonists, some of which demonstrate bias for G protein activation over β-arrestin2 recruitment.

View Article and Find Full Text PDF

Two-step ligand exchange to promote charge transfer in PbSe quantum dot photodetectors for pulse monitoring.

Nanoscale Horiz

September 2025

State Key Laboratory of Electronic Thin Films and Integrated Devices, School of Optoelectronic Science and Engineering, University of Electronic Science and Technology of China (UESTC), Chengdu 611731, China.

Quantum dots (QDs) have emerged as promising materials for next-generation infrared semiconductors due to their facile solution processing, low-cost, tunable bandgap and superior optoelectronic properties. However, organic long-chain ligands that modify the surface of QDs hinder charge transfer, thus impairing the performance of QD infrared photodetectors. Here, we report a two-step ligand exchange strategy that decouples the native long-chain ligands from the QDs using specific molecules and then attaches the short-chain ligands, resulting in high response for lead-rich lead selenide (PbSe) QD photodetectors.

View Article and Find Full Text PDF

Tuning of G-CSFR signaling by de novo designed agonists.

Mol Ther

August 2025

Max Planck Institute for Biology, Department Protein Evolution, 72076 Tübingen, Germany; Friedrich Miescher Laboratory of the Max Planck Society, 72076 Tübingen, Germany; Internal Medicine II, University Hospital Tübingen, 72076 Tübingen, Germany. Electronic address:

Enhancing cytokine-based therapies by systematically tuning how an agonist associates its receptor is emerging as a powerful new concept in drug discovery. Here, we report the design and characterization of agonists that tune the granulocyte-colony stimulating factor receptor (G-CSFR) activity, which is central for the proliferation and granulocytic differentiation of hematopoietic stem cells. Using design agonists, we study the impact of varying the receptor-binding affinity and dimerization geometry on receptor association, downstream signaling, and cellular response.

View Article and Find Full Text PDF

Quantum dots (QDs) are semiconductor nanocrystals with stable and bright fluorescence, attributes particularly valued for single-molecule imaging in the life sciences. For these applications, QDs must be compact and homogeneously dispersed as single colloids, attributes enabled by multidentate polymer coatings. However, high-resolution analyses show evidence of clusters of two or more QDs (multimers) that may dominate measurements at the single-particle level.

View Article and Find Full Text PDF

Synthetic cannabinoid receptor agonists (SCRAs) are a class of novel psychoactive substances whose prevalence in illegal markets continues to grow. Δ-tetrahydrocannabinol (THC) is the primary intoxicating compound present in cannabis and is well-known to behave as a partial agonist at both the type 1 and 2 cannabinoid receptors (CB1R, CB2R). Unlike THC, the SCRAs characterized to date generally behave as CB1R and/or CB2R full agonists.

View Article and Find Full Text PDF