Evidence map›Paper›PMID 23280114›Full record

ArticleMethods in enzymology2013

Fluctuation analysis of activity biosensor images for the study of information flow in signaling pathways.

Marco Vilela, Nadia Halidi, Sebastien Besson, Hunter Elliott, Klaus Hahn, Jessica Tytell, Gaudenz Danuser

Abstract read
In one paragraph

Article in Methods in enzymology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing 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

19 citing papers in PubMed.

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  4. Discovery of functional interactions among actin regulators by analysis of image fluctuations in an unperturbed motile cell system.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2018
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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

7 authors.

Marco VilelaDepartment of Cell Biology, Harvard Medical School, Boston, Massachusetts, USA.
Nadia Halidi
Sebastien Besson
Hunter Elliott
Klaus Hahn
Jessica Tytell
Gaudenz Danuser

Funding

Quantitative Imaging of Signaling NetworksR01GM090317 · NIGMS · HARVARD MEDICAL SCHOOL · PI DANUSER, GAUDENZ, HAHN, KLAUS M. · 2009 to 2013
$3.4M
Signaling network reconstruction from biosensor image fluctuationsF32GM103278 · NIGMS · HARVARD MEDICAL SCHOOL · PI VILELA, MARCO ANTONIO · 2012 to 2014
$80k
NIGMS NIH HHS F32 GM103278NIGMS NIH HHS R01 GM090317NIGMS NIH HHS T-R01 GM090317
6 · The paper itself

Abstract

Comprehensive understanding of cellular signal transduction requires accurate measurement of the information flow in molecular pathways. In the past, information flow has been inferred primarily from genetic or protein-protein interactions. Although useful for overall signaling, these approaches are limited in that they typically average over populations of cells. Single-cell data of signaling states are emerging, but these data are usually snapshots of a particular time point or limited to averaging over a whole cell. However, many signaling pathways are activated only transiently in specific subcellular regions. Protein activity biosensors allow measurement of the spatiotemporal activation of signaling molecules in living cells. These data contain highly complex, dynamic information that can be parsed out in time and space and compared with other signaling events as well as changes in cell structure and morphology. We describe in this chapter the use of computational tools to correct, extract, and process information from time-lapse images of biosensors. These computational tools allow one to explore the biosensor signals in a multiplexed approach in order to reconstruct the sequence of signaling events and consequently the topology of the underlying pathway. The extraction of this information, dynamics and topology, provides insight into how the inputs of a signaling network are translated into its biochemical or mechanical outputs.

Indexed as

Biosensing TechniquesSignal TransductionAffinity LabelsCell ShapeAffinity Labels

Identifiers

PMID23280114
PMCPMC4174660

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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.