Evidence map›Paper›PMID 30062413›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2018

Small-Volume Flow Cytometry-Based Multiplex Analysis of the Activity of Small GTPases.

Peter Simons, Virginie Bondu, Angela Wandinger-Ness, Tione Buranda

Open access · hybridAbstract read
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 31% of its field
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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Heterozygous variants in DOCK2 leading to susceptibility to viral illnesses.The Journal of allergy and clinical immunology · 2026
    Article
  2. A model for predicting bacteremia species based on host immune response.Frontiers in cellular and infection microbiology · 2025
    Article
  3. Article
  4. Review
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

4 authors at 1 institution in 1 country.

Peter SimonsDepartment of Pathology, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Virginie BonduDepartment of Pathology, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Angela Wandinger-NessDepartment of Pathology, University of New Mexico School of Medicine, Albuquerque, NM, USA.
Tione BurandaDepartment of Pathology, University of New Mexico School of Medicine, Albuquerque, NM, USA. tburanda@salud.unm.edu.
University of New Mexico · US

Funding

Spatiotemporal Regulation of Membrane Raft Trafficking in Virus Activated CellsR03AI092130 · NIAID · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BURANDA, TIONE · 2011 to 2012
$151k
Development of HTS Assays for Inhibitors of Viral-Cell InteractionsR21NS066429 · NINDS · UNIVERSITY OF NEW MEXICO HEALTH SCIS CTR · PI BURANDA, TIONE · 2010 to 2010
$151k
HTS to identify small molecules that disrupt Rab GTPase activator and effector prR21NS066435 · NINDS · UNIVERSITY OF NEW MEXICO · PI WANDINGER-NESS, ANGELA · 2009 to 2009
$149k
NIAID NIH HHS R03 AI092130NINDS NIH HHS R21 NS066429NINDS NIH HHS R21 NS066435
6 · The paper itself

Abstract

Small, monomeric guanine triphosphate hydrolases (GTPases) are ubiquitous cellular integrators of signaling. A signal activates the GTPase, which then binds to an effector molecule to relay a signal inside the cell. The GTPase effector trap flow cytometry assay (G-Trap) utilizes bead-based protein immobilization and dual-color flow cytometry to rapidly and quantitatively measure GTPase activity status in cell or tissue lysates. Beginning with commercial cytoplex bead sets that are color-coded with graded fluorescence intensities of a red (700 nm) wavelength, the bead sets are derivatized to display glutathione on the surface through a detailed protocol described here. A different glutathione-S-transferase-effector protein (GST-effector protein) can then be attached to the surface of each set. For the assay, users can incubate bead sets individually or in a multiplex format with lysates for rapid, selective capture of active, GTP-bound GTPases from a single sample. After that, flow cytometry is used to identify the bead-borne GTPase based on red bead intensity, and the amount of active GTPase per bead is detected using monoclonal antibodies conjugated to a green fluorophore or via labeled secondary antibodies. Three examples are provided to illustrate the efficacy of the effector-functionalized beads for measuring the activation of at least five GTPases in a single lysate from fewer than 50,000 cells.

Indexed as

AnimalsAntibodies, MonoclonalCell LineFlow CytometryFluorescent DyesGlutathione TransferaseGTP PhosphohydrolasesGuanosine TriphosphateHumansAntibodies, MonoclonalFluorescent DyesGlutathione TransferaseGTP PhosphohydrolasesGuanosine TriphosphateArgatrobanBead functionalizationCell signalingCytoskeletonFlow cytometryFluorescence calibration beadsGlutathione-S-transferase (GST)GTPase effector beadsHantavirusIntegrin activationMultiplexProtease-activated receptors (PARs)Rab7Rab GTPaseRac1Rap1RhoARho GTPaseSepsisThrombin

Identifiers

PMID30062413
PMCPMC6462310
OpenAlexW2886842371

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.