Evidence map›Paper›PMID 24391085›Full record

ArticleCurrent protocols in chemical biology2013

Using a kinase-inducible bimolecular switch to control enzyme activity in living cells.

Sohum Mehta, Jin Zhang

Abstract read
In one paragraph

Article in Current protocols in chemical biology, 2013. 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.

Sohum MehtaDepartment of Pharmacology and Molecular Sciences, The Johns Hopkins University School of Medicine, Baltimore, Maryland.
Jin Zhang

Funding

Mechanisms of Compartmentalized cAMP SignalingR01DK073368 · NIDDK · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI Jin Zhang · 2006 to 2026
$7.6M
Creating a Genetically Encodable Nano-Compass to Navigate in Molecular NetworksDP1CA174423 · NCI · UNIVERSITY OF CALIFORNIA, SAN DIEGO · PI ZHANG, JIN · 2012 to 2014
$1.6M
NCI NIH HHS DP1 CA174423NIDDK NIH HHS R01 DK073368
6 · The paper itself

Abstract

Molecular switches have been instrumental in the development of powerful and versatile genetic tools for directly probing biochemical processes, such as intracellular signaling, within their native contexts. A molecular switch can be broadly defined as a molecular system capable of existing in either of two states (e.g., conformations), which can be converted from one state to the other by a specific input stimulus. This protocol outlines a method for using a kinase-inducible bimolecular switch, along with live-cell fluorescence microscopy, to directly control and monitor the activity of a specific enzyme in living cells.

Indexed as

Cell LineCell Physiological PhenomenaDNAGenes, SwitchHumansIndicators and ReagentsMicroscopy, FluorescencePhosphotransferasesSignal TransductionDNAIndicators and ReagentsPhosphotransferasesbiochemical perturbationbiosensorfluorescencelive-cell imaging

Identifiers

PMID24391085
PMCPMC3989098

What OpenQuestion holds

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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.