Evidence map›Paper›PMID 32763980›Full record

ArticleThe Plant cell2020

Covalent Self-Labeling of Tagged Proteins with Chemical Fluorescent Dyes in BY-2 Cells and Arabidopsis Seedlings.

Ryu J Iwatate, Akira Yoshinari, Noriyoshi Yagi, Marek Grzybowski, Hiroaki Ogasawara, Mako Kamiya, Toru Komatsu, Masayasu Taki, Shigehiro Yamaguchi, Wolf B Frommer and 1 more

Open access · greenAbstract read
In one paragraph

Article in The Plant cell, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
1.6field-weighted citation impact, top 17% 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

18 citing papers in PubMed, 35 citations in OpenAlex.

  1. Article
  2. Article
  3. SNAP-Tech 2.0.Nature chemical biology · 2025
    Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. A novel toolbox to record CLE peptide signaling.Frontiers in plant science · 2024
    Article
  9. Review
  10. Article
  11. Review
  12. Review
  13. Article
  14. Article
  15. Review
  16. Single-Molecule Imaging in Living Plant Cells: A Methodological Review.International journal of molecular sciences · 2021
    Review
  17. Article
  18. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

11 authors at 3 institutions in 2 countries.

Ryu J IwatateInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan.ORCID 0000-0001-6111-7809
Akira YoshinariInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan.ORCID 0000-0002-7083-5674
Noriyoshi YagiInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan.ORCID 0000-0002-2827-6362
Marek GrzybowskiInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan.ORCID 0000-0001-6678-4950
Hiroaki OgasawaraInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan.ORCID 0000-0001-8462-562X
Mako KamiyaGraduate School of Medicine, University of Tokyo, Tokyo 113-0033, Japan.ORCID 0000-0002-5592-1849
Toru KomatsuPrecursory Research for Embryonic Science and Technology (PRESTO), Japan Science and Technology Agency, Kawaguchi, Saitama 332-0012, Japan.ORCID 0000-0002-9268-6964
Masayasu TakiInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan.ORCID 0000-0003-2185-4593
Shigehiro YamaguchiInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan.ORCID 0000-0003-0072-8969
Wolf B FrommerInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan mnakamu@itbm.nagoya-u.ac.jp wfrommer@itbm.nagoya-u.ac.jp.ORCID 0000-0001-6465-0115
Masayoshi NakamuraInstitute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Chikusa, Nagoya 464-8601, Japan mnakamu@itbm.nagoya-u.ac.jp wfrommer@itbm.nagoya-u.ac.jp.ORCID 0000-0002-7107-4942
Nagoya University · JPJapan Science and Technology Agency · JPHeinrich Heine University Düsseldorf · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synthetic chemical fluorescent dyes promise to be useful for many applications in biology. Covalent, targeted labeling, such as with a SNAP-tag, uses synthetic dyes to label specific proteins in vivo for studying processes such as endocytosis or for imaging via super-resolution microscopy. Despite its potential, such chemical tagging has not been used effectively in plants. A major drawback has been the limited knowledge regarding cell wall and membrane permeability of the available synthetic dyes. Of 31 synthetic dyes tested here, 23 were taken up into BY-2 cells, while eight were not. This creates sets of dyes that can serve to measure endocytosis. Three of the dyes that were able to enter the cells, SNAP-tag ligands of diethylaminocoumarin, tetramethylrhodamine, and silicon-rhodamine 647, were used to SNAP-tag α-tubulin. Successful tagging was verified by live cell imaging and visualization of microtubule arrays in interphase and during mitosis in Arabidopsis (

Indexed as

ArabidopsisArabidopsis ProteinsEndocytosisFluorescent DyesMicrotubule-Associated ProteinsO(6)-Methylguanine-DNA MethyltransferasePlant CellsPlants, Genetically ModifiedRhodaminesSeedlingsTime-Lapse ImagingTubulinArabidopsis ProteinsAT5G57090 protein, ArabidopsisFluorescent DyesMicrotubule-Associated ProteinsO(6)-Methylguanine-DNA MethyltransferaseRhodaminesSPIRAL2 protein, ArabidopsistetramethylrhodamineTubulin

Identifiers

PMID32763980
PMCPMC7534461
OpenAlexW3047708087

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.