Evidence map›Paper›PMID 24798463›Full record

ArticlePloS one2014

A new genetically encoded single-chain biosensor for Cdc42 based on FRET, useful for live-cell imaging.

Samer Hanna, Veronika Miskolci, Dianne Cox, Louis Hodgson

Open access · goldAbstract readValidation Study
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

33 citing papers in PubMed, 49 citations in OpenAlex.

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  12. Multiplex Imaging of Rho GTPase Activities in Living Cells.Methods in molecular biology (Clifton, N.J.) · 2021
    Article
  13. Article
  14. Vav2 lacks CaJournal of cell science · 2020
    Article
  15. Optogenetics: Rho GTPases Activated by Light in Living Macrophages.Methods in molecular biology (Clifton, N.J.) · 2020
    Article
  16. Textures of the tumour microenvironment.Essays in biochemistry · 2019
    Review
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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 2 institutions in 1 country.

Samer HannaDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, United States of America.
Veronika MiskolciDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, United States of America.
Dianne CoxDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, United States of America; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, United States of America.
Louis HodgsonDepartment of Anatomy and Structural Biology, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, United States of America; Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine of Yeshiva University, Bronx, New York, United States of America.
Albert Einstein College of Medicine · USYeshiva University · US

Funding

WORD PROCESSORP30CA013330 · NCI · YESHIVA UNIVERSITY · PI THOMAS E ROHAN · 1985 to 2026
$111.2M
TRAINING PROGRAM IN CELLULAR &MOLEC. BIOLOGY &GENETICST32GM007491 · NIGMS · YESHIVA UNIVERSITY · PI QUERY, CHARLES C · 1985 to 2021
$17.0M
THE ROLE OF CSF-1 MEDIATED MACROPHAGE CHEMOTAXIS IN CARCINOMA CELL INVASIONR01GM071828 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI COX, DIANNE · 2006 to 2014
$2.9M
RhoC GTPase regulates leading edge protrusion dynamics in breast carcinomasR01GM093121 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE · PI HODGSON, LOUIS · 2010 to 2014
$1.6M
NCI NIH HHS P30 CA013330NIGMS NIH HHS GM071828NIGMS NIH HHS GM093121NIGMS NIH HHS R01 GM071828NIGMS NIH HHS R01 GM093121NIGMS NIH HHS T32 GM007491NIGMS NIH HHS T32GM007491
6 · The paper itself

Abstract

Cdc42 is critical in a myriad of cellular morphogenic processes, requiring precisely regulated activation dynamics to affect specific cellular events. To facilitate direct observations of Cdc42 activation in live cells, we developed and validated a new biosensor of Cdc42 activation. The biosensor is genetically encoded, of single-chain design and capable of correctly localizing to membrane compartments as well as interacting with its upstream regulators including the guanine nucleotide dissociation inhibitor. We characterized this new biosensor in motile mouse embryonic fibroblasts and observed robust activation dynamics at leading edge protrusions, similar to those previously observed for endogenous Cdc42 using the organic dye-based biosensor system. We then extended our validations and observations of Cdc42 activity to macrophages, and show that this new biosensor is able to detect differential activation patterns during phagocytosis and cytokine stimulation. Furthermore, we observe for the first time, a highly transient and localized activation of Cdc42 during podosome formation in macrophages, which was previously hypothesized but never directly visualized.

Indexed as

Biosensing TechniquesAnimalscdc42 GTP-Binding ProteinCells, CulturedFluorescence Resonance Energy TransferFluorometryMiceNIH 3T3 Cellscdc42 GTP-Binding Protein

Identifiers

PMID24798463
PMCPMC4010534
OpenAlexW2022717766

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.