Evidence map›Paper›PMID 26444439›Full record

ArticleJournal of microscopy2016

Important factors determining the nanoscale tracking precision of dynamic microtubule ends.

G Bohner, N Gustafsson, N I Cade, S P Maurer, L D Griffin, T Surrey

Abstract read
In one paragraph

Article in Journal of microscopy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing 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

12 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Review
  5. Review
  6. Article
  7. Article
  8. Measuring microtubule dynamics.Essays in biochemistry · 2018
    Review
  9. Article
  10. Steady-state EB cap size fluctuations are determined by stochastic microtubule growth and maturation.Proceedings of the National Academy of Sciences of the United States of America · 2017
    Article
  11. Article
  12. Article
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.

G BohnerThe Francis Crick Institute, Lincoln's Inn Fields Laboratory, London, U.K.
N GustafssonCentre for Mathematics and Physics in Life Sciences and Experimental Biology (CoMPLEX), University College London, London, U.K.
N I CadeThe Francis Crick Institute, Lincoln's Inn Fields Laboratory, London, U.K.
S P MaurerThe Francis Crick Institute, Lincoln's Inn Fields Laboratory, London, U.K.
L D GriffinCentre for Mathematics and Physics in Life Sciences and Experimental Biology (CoMPLEX), University College London, London, U.K.
T SurreyThe Francis Crick Institute, Lincoln's Inn Fields Laboratory, London, U.K.

Funding

Cancer Research UK 14256
6 · The paper itself

Abstract

Tracking dynamic microtubule ends in fluorescence microscopy movies provides insight into the statistical properties of microtubule dynamics and is vital for further analysis that requires knowledge of the trajectories of the microtubule ends. Here we analyse the performance of a previously developed automated microtubule end tracking routine; this has been optimized for comparatively low signal-to-noise image sequences that are characteristic of microscopy movies of dynamic microtubules growing in vitro. Sequences of simulated microtubule images were generated assuming a variety of different experimental conditions. The simulated movies were then tracked and the tracking errors were characterized. We found that the growth characteristics of the microtubules within realistic ranges had a negligible effect on the tracking precision. The fluorophore labelling density, the pixel size of the images, and the exposure times were found to be important parameters limiting the tracking precision which could be explained using concepts of single molecule localization microscopy. The signal-to-noise ratio was found to be a good single predictor of the tracking precision: typical experimental signal-to-noise ratios lead to tracking precisions in the range of tens of nanometres, making the tracking program described here a useful tool for dynamic microtubule end tracking with close to molecular precision.

Indexed as

AlgorithmsComputer SimulationFluorescent DyesImage Processing, Computer-AssistedMicroscopy, FluorescenceMicrotubulesFluorescent DyesImage processingimage simulationmicrotubuleTIRF microscopytracking

Identifiers

PMID26444439
PMCPMC4832305

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Registered trials

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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.