Evidence map›Paper›PMID 25968318›Full record

ArticleDevelopment (Cambridge, England)2015

Live imaging of endogenous protein dynamics in zebrafish using chromobodies.

Paolo Panza, Julia Maier, Christian Schmees, Ulrich Rothbauer, Christian Söllner

Abstract read
In one paragraph

Article in Development (Cambridge, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 52 papers.

0numbers the graph read from it
0cells of the map it votes in
52citing 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

52 citing papers in PubMed.

  1. Review
  2. Article
  3. SiR-XActin: A Fluorescent Probe for Imaging Actin Dynamics in Live Cells.Angewandte Chemie (International ed. in English) · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. bioRxiv : the preprint server for biology · 2023
    Article
  8. Article
  9. Article
  10. Antibody-Based Approaches to Target Pancreatic Tumours.Antibodies (Basel, Switzerland) · 2022
    Review
  11. Article
  12. Article
  13. Peptide-Tag Specific Nanobodies for Studying Proteins in Live Cells.Methods in molecular biology (Clifton, N.J.) · 2022
    Article
  14. Article
  15. Article
  16. Article
  17. Review
  18. Article
  19. Review
  20. Tools of the trade: studying actin in zebrafish.Histochemistry and cell biology · 2020
    Review
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

5 authors.

Paolo PanzaMax-Planck-Institut für Entwicklungsbiologie, Abteilung Genetik, Spemannstraße 35, Tübingen 72076, Germany paolo.panza@tuebingen.mpg.de.
Julia MaierNaturwissenschaftliches und Medizinisches Institut der Universität Tübingen, Markwiesenstraße 55, Reutlingen 72770, Germany Pharmazeutische Biotechnologie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 8, Tübingen 72076, Germany.
Christian SchmeesNaturwissenschaftliches und Medizinisches Institut der Universität Tübingen, Markwiesenstraße 55, Reutlingen 72770, Germany.
Ulrich RothbauerNaturwissenschaftliches und Medizinisches Institut der Universität Tübingen, Markwiesenstraße 55, Reutlingen 72770, Germany Pharmazeutische Biotechnologie, Eberhard Karls Universität Tübingen, Auf der Morgenstelle 8, Tübingen 72076, Germany.
Christian SöllnerMax-Planck-Institut für Entwicklungsbiologie, Abteilung Genetik, Spemannstraße 35, Tübingen 72076, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chromobodies are intracellular nanoprobes that combine the specificity of antibodies with the convenience of live fluorescence imaging in a flexible, DNA-encoded reagent. Here, we present the first application of this technique to an intact living vertebrate organism. We generated zebrafish lines expressing chromobodies that trace the major cytoskeletal component actin and the cell cycle marker PCNA with spatial and temporal specificity. Using these chromobodies, we captured full localization dynamics of the endogenous antigens in different cell types and at different stages of development. For the first time, the chromobody technology enables live imaging of endogenous subcellular structures in an animal, with the remarkable advantage of avoiding target protein overexpression or tagging. In combination with improved chromobody selection systems, we anticipate a rapid adaptation of this technique to new intracellular antigens and model organisms, allowing the faithful description of cellular and molecular processes in their dynamic state.

Indexed as

ActinsAnimalsCell CycleDiagnostic ImagingSingle-Domain AntibodiesZebrafishZebrafish ProteinsActinsSingle-Domain AntibodiesZebrafish ProteinsActinLive imagingNanobodyPCNAProtein dynamics

Identifiers

PMID25968318
PMCPMC4440926

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.