Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Analysis of Arrestin Recruitment to Chemokine Receptors by Bioluminescence Resonance Energy Transfer.

Methods in enzymology - 1 Jan 2016

Bonneterre J, Montpas N, Boularan C, Galés C, Heveker N

Abstract excerpt

Chemokine receptors recruit the multifunctional scaffolding protein beta arrestin in response to binding of their chemokine ligands. Given that arrestin recruitment represents a signaling axis that is in part independent from G-protein signaling, it has become a hallmark of G protein-coupled receptor functional selectivity. Therefore, quantification of arrestin recruitment has become a requirement for the...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Arrestins
Share to Chemokines
Share to Dose-Response Relationship, Drug

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Ligands

Share to Mutation

Share to Protein Interaction Mapping

Share to Receptors, Chemokine

Share to Recombinant Proteins

Source

Identifiers

PMID: 26921945
DOI: 10.1016/bs.mie.2015.09.003

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Analysis of Arrestin Recruitment to Chemokine Receptors by Bioluminescence Resonance Energy Transfer.PMID 26921945Read ↗

A novel approach to quantify G-protein-coupled receptor dimerization equilibrium using bioluminescence resonance energy transfer.Semantic proximity Read ↗

Receptor-Arrestin Interactions: The GPCR Perspective.Semantic proximity Read ↗

Heptahelical terpsichory. Who calls the tune?Semantic proximity Read ↗

A rapid fluorogenic GPCR-β-arrestin interaction assay.Semantic proximity Read ↗

β-Arrestins 1 and 2 are critical regulators of inflammationSemantic proximity Read ↗

Conformational selection guides β-arrestin recruitment at a biased G protein-coupled receptor.Semantic proximity Read ↗

Structural basis for chemokine recognition by a G protein-coupled receptor and implications for receptor activation.Semantic proximity Read ↗

Activation and nuclear translocation of ERK1/2 by the formyl peptide receptor is regulated by G protein and is not dependent on beta-arrestin translocation or receptor endocytosis.Semantic proximity Read ↗

A Model for the Signal Initiation Complex Between Arrestin-3 and the Src Family Kinase Fgr.Semantic proximity Read ↗

Recent progress in assays for GPCR drug discoverySemantic proximity Read ↗

CXCR7 Controls Competition for Recruitment of β-Arrestin 2 in Cells Expressing Both CXCR4 and CXCR7Semantic proximity Read ↗

Quantitative assessment of constitutive G protein-coupled receptor activity with BRET-based G protein biosensorsSemantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.