Evidence map›Paper›PMID 31311871›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2019

A real-time, click chemistry imaging approach reveals stimulus-specific subcellular locations of phospholipase D activity.

Dongjun Liang, Kane Wu, Reika Tei, Timothy W Bumpus, Johnny Ye, Jeremy M Baskin

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 56 papers.

0numbers the graph read from it
0cells of the map it votes in
56citing papers in PubMed
4.1field-weighted citation impact, top 5% 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

56 citing papers in PubMed, 94 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Review
  5. bioRxiv : the preprint server for biology · 2026
    Article
  6. Subcellular Cartography of the Phosphoinositide Multiverse.Biochimica et biophysica acta. Molecular and cell biology of lipids · 2026
    Review
  7. Article
  8. Article
  9. Article
  10. A Fluorogenic Hydrazino-Pictet-Spengler Reaction in Live Cells.Angewandte Chemie (International ed. in English) · 2025
    Article
  11. Article
  12. Review
  13. Article
  14. Synthetic Lipid Biology.Chemical reviews · 2025
    Review
  15. Article
  16. Article
  17. Review
  18. Article
  19. Probing Glycerolipid Metabolism using a Caged Clickable Glycerol-3-Phosphate Probe.Chembiochem : a European journal of chemical biology · 2024
    Article
  20. Optogenetic Strategies for Optimizing the Performance of Phospholipids Biosensors.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024
    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 1 institution in 1 country.

Dongjun LiangDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853.ORCID 0000-0003-0200-7364
Kane WuDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853.
Reika TeiDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853.ORCID 0000-0002-9492-9309
Timothy W BumpusDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853.ORCID 0000-0001-5866-5361
Johnny YeDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853.
Jeremy M BaskinDepartment of Chemistry and Chemical Biology, Cornell University, Ithaca, NY 14853; jeremy.baskin@cornell.edu.ORCID 0000-0003-2939-3138
Cornell University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The fidelity of signal transduction requires spatiotemporal control of the production of signaling agents. Phosphatidic acid (PA) is a pleiotropic lipid second messenger whose modes of action differ based on upstream stimulus, biosynthetic source, and site of production. How cells regulate the local production of PA to effect diverse signaling outcomes remains elusive. Unlike other second messengers, sites of PA biosynthesis cannot be accurately visualized with subcellular precision. Here, we describe a rapid, chemoenzymatic approach for imaging physiological PA production by phospholipase D (PLD) enzymes. Our method capitalizes on the remarkable discovery that bulky, hydrophilic

Indexed as

Imaging, Three-DimensionalAnimalsCell MembraneClick ChemistryEndoplasmic ReticulumFluorescent DyesHeLa CellsHumansLipidsMiceNIH 3T3 CellsPhosphatidic AcidsPhospholipase DReceptor, Muscarinic M1Receptors, Platelet-Derived Growth FactorSubcellular FractionsFluorescent DyesLipidsPhosphatidic AcidsPhospholipase DReceptor, Muscarinic M1Receptors, Platelet-Derived Growth Factorclick chemistrylipid traffickingphosphatidic acidphospholipase Dsecond messengers

Identifiers

PMID31311871
PMCPMC6681737
OpenAlexW2956842188

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.