Evidence map›Paper›PMID 29379139›Full record

ArticleNature cell biology2018

Local control of intracellular microtubule dynamics by EB1 photodissociation.

Jeffrey van Haren, Rabab A Charafeddine, Andreas Ettinger, Hui Wang, Klaus M Hahn, Torsten Wittmann

Abstract readVideo-Audio Media
In one paragraph

Article in Nature cell biology, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
5.3field-weighted citation impact, top 4% 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

45 citing papers in PubMed, 88 citations in OpenAlex.

  1. Article
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  10. Therapeutic gene silencing ofScience advances · 2023
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  13. Review
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  19. Journal of the American Chemical Society · 2022
    Article
  20. 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 at 2 institutions in 2 countries.

Jeffrey van HarenDepartment of Cell and Tissue Biology, University of California, San Francisco, CA, USA.
Rabab A CharafeddineDepartment of Cell and Tissue Biology, University of California, San Francisco, CA, USA.
Andreas EttingerDepartment of Cell and Tissue Biology, University of California, San Francisco, CA, USA.
Hui WangUniversity of North Carolina, Chapel Hill, NC, USA.
Klaus M HahnUniversity of North Carolina, Chapel Hill, NC, USA.
Torsten WittmannDepartment of Cell and Tissue Biology, University of California, San Francisco, CA, USA. torsten.wittmann@ucsf.edu.ORCID http://orcid.org/0000-0001-9134-691X
University of California, San Francisco · USUniversity of North Carolina at Chapel Hill · US

Funding

Virology Research Program (Program 4)P30CA016086 · NCI · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Deborah F. Tate · 1985 to 2026
$201.5M
INTERACTIVE GRAPHICS FOR MOLECULAR STUDIES &MICROSCOPYP41EB002025 · NIBIB · UNIV OF NORTH CAROLINA CHAPEL HILL · PI SUPERFINE, RICHARD · 2003 to 2019
$16.9M
Dissecting signaling in vivo via precise control and visualization of protein activityR35GM122596 · NIGMS · UNIV OF NORTH CAROLINA CHAPEL HILL · PI Klaus M. Hahn · 2017 to 2026
$7.4M
Microtubule dynamics during cell polarity and migrationR01GM079139 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WITTMANN, TORSTEN · 2008 to 2017
$2.7M
Light-activated proteolysis as a tool to analyze intracellular protein functionR01GM094819 · NIGMS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WITTMANN, TORSTEN · 2010 to 2013
$1.2M
Spinning disk confocal / FRAP microscope for quantitative live cell imagingS10RR026758 · NCRR · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI WITTMANN, TORSTEN · 2010 to 2010
$500k
NCI NIH HHS P30 CA016086NCRR NIH HHS S10 RR026758NIBIB NIH HHS P41 EB002025NIGMS NIH HHS R01 GM079139NIGMS NIH HHS R01 GM094819NIGMS NIH HHS R35 GM122596
6 · The paper itself

Abstract

End-binding proteins (EBs) are adaptors that recruit functionally diverse microtubule plus-end-tracking proteins (+TIPs) to growing microtubule plus ends. To test with high spatial and temporal accuracy how, when and where +TIP complexes contribute to dynamic cell biology, we developed a photo-inactivated EB1 variant (π-EB1) by inserting a blue-light-sensitive protein-protein interaction module between the microtubule-binding and +TIP-binding domains of EB1. π-EB1 replaces endogenous EB1 function in the absence of blue light. By contrast, blue-light-mediated π-EB1 photodissociation results in rapid +TIP complex disassembly, and acutely and reversibly attenuates microtubule growth independent of microtubule end association of the microtubule polymerase CKAP5 (also known as ch-TOG and XMAP215). Local π-EB1 photodissociation allows subcellular control of microtubule dynamics at the second and micrometre scale, and elicits aversive turning of migrating cancer cells. Importantly, light-mediated domain splitting can serve as a template to optically control other intracellular protein activities.

Indexed as

Cell MovementOptogeneticsCarcinoma, Non-Small-Cell LungCell Line, TumorHumansLung NeoplasmsMicroscopy, FluorescenceMicrotubule-Associated ProteinsMicrotubulesPhotolysisProtein BindingProtein Interaction Domains and MotifsSignal TransductionTime FactorsTime-Lapse ImagingCKAP5 protein, humanMAPRE1 protein, humanMicrotubule-Associated Proteins

Identifiers

PMID29379139
PMCPMC5826794
OpenAlexW2792066084

What OpenQuestion holds

Textmetadata
LicenceTDM
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.