Evidence map›Paper›PMID 21961607›Full record

ArticleBiophysical journal2011

Interactive, computer-assisted tracking of speckle trajectories in fluorescence microscopy: application to actin polymerization and membrane fusion.

Matthew B Smith, Erdem Karatekin, Andrea Gohlke, Hiroaki Mizuno, Naoki Watanabe, Dimitrios Vavylonis

Open access · bronzeAbstract read
In one paragraph

Article in Biophysical journal, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
8.9field-weighted citation impact, top 3% 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

39 citing papers in PubMed, 86 citations in OpenAlex.

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  9. Retromer forms low order oligomers on supported lipid bilayers.The Journal of biological chemistry · 2020
    Article
  10. Article
  11. Lamellipodium tip actin barbed ends serve as a force sensor.Genes to cells : devoted to molecular & cellular mechanisms · 2019
    Article
  12. Article
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  16. Helical rotation of the diaphanous-related formin mDia1 generates actin filaments resistant to cofilin.Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
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  19. 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

6 authors at 4 institutions in 3 countries.

Matthew B SmithDepartment of Physics, Lehigh University, Bethlehem, Pennsylvania, USA.
Erdem Karatekin
Andrea Gohlke
Hiroaki Mizuno
Naoki Watanabe
Dimitrios Vavylonis
Lehigh University · USTohoku University · JPDélégation Paris 5 · FRYale University · US

Funding

Computational Analysis and Modeling of Contractile Ring AssemblyR21GM083928 · NIGMS · LEHIGH UNIVERSITY · PI HUANG, SHARON XIAOLEI, VAVYLONIS, DIMITRIOS · 2008 to 2009
$386k
NIGMS NIH HHS R21 GM083928NIGMS NIH HHS R21GM083928
6 · The paper itself

Abstract

Analysis of particle trajectories in images obtained by fluorescence microscopy reveals biophysical properties such as diffusion coefficient or rates of association and dissociation. Particle tracking and lifetime measurement is often limited by noise, large mobilities, image inhomogeneities, and path crossings. We present Speckle TrackerJ, a tool that addresses some of these challenges using computer-assisted techniques for finding positions and tracking particles in different situations. A dynamic user interface assists in the creation, editing, and refining of particle tracks. The following are results from application of this program: 1), Tracking single molecule diffusion in simulated images. The shape of the diffusing marker on the image changes from speckle to cloud, depending on the relationship of the diffusion coefficient to the camera exposure time. We use these images to illustrate the range of diffusion coefficients that can be measured. 2), We used the program to measure the diffusion coefficient of capping proteins in the lamellipodium. We found values ∼0.5 μm(2)/s, suggesting capping protein association with protein complexes or the membrane. 3), We demonstrate efficient measuring of appearance and disappearance of EGFP-actin speckles within the lamellipodium of motile cells that indicate actin monomer incorporation into the actin filament network. 4), We marked appearance and disappearance events of fluorescently labeled vesicles to supported lipid bilayers and tracked single lipids from the fused vesicle on the bilayer. This is the first time, to our knowledge, that vesicle fusion has been detected with single molecule sensitivity and the program allowed us to perform a quantitative analysis. 5), By discriminating between undocking and fusion events, dwell times for vesicle fusion after vesicle docking to membranes can be measured.

Indexed as

Membrane FusionProtein MultimerizationUser-Computer InterfaceActin Capping ProteinsActinsAnimalsCell LineCell MovementDiffusionFluorescent DyesLipid BilayersLiposomesMicroscopy, FluorescenceProtein Structure, QuaternaryPseudopodiaSNARE ProteinsActin Capping ProteinsActinsFluorescent DyesLipid BilayersLiposomesSNARE Proteins

Identifiers

PMID21961607
PMCPMC3183794
OpenAlexW1987739173

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.