Evidence map›Paper›PMID 42156698›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2026

A Comprehensive Approach to Monitor Endocytosis and Trafficking of G Protein-Coupled Receptors: Tools for Exploring Receptor-Lipid Interaction.

Ashwani Sharma, Amitabha Chattopadhyay

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

2 authors.

Ashwani SharmaCSIR-Centre for Cellular and Molecular Biology, Hyderabad, India.
Amitabha ChattopadhyayCSIR-Centre for Cellular and Molecular Biology, Hyderabad, India. amit.ccmb@csir.res.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

G protein-coupled receptors (GPCRs) are cellular nanomachines that act as signaling hubs and account for ~40% of current drug targets. Endocytosis of GPCRs represents a major regulatory mechanism to sustain their downstream signaling within a stringent spatiotemporal regime. This is achieved by internalizing a fraction of the plasma membrane receptor population, thereby reducing the available pool of receptors for signaling at the cell membrane. In this article, we describe a detailed step-by-step hands-on guide that we have successfully used to monitor GPCR endocytosis and intracellular trafficking using serotonin

Indexed as

EndocytosisMembrane LipidsReceptor, Serotonin, 5-HT1AReceptors, G-Protein-CoupledAnimalsCell MembraneCholesterolFlow CytometryHEK293 CellsHumansMicroscopy, ConfocalProtein TransportCholesterolMembrane LipidsReceptor, Serotonin, 5-HT1AReceptors, G-Protein-CoupledCholesterolConfocal microscopyEndocytosisFlow cytometryGPCRMembrane lipidsQuantitative colocalizationSerotonin1A receptorTrafficking

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.