Evidence map›Paper›PMID 30850602›Full record

ArticleNature communications2019

Neurotrophin receptor tyrosine kinases regulated with near-infrared light.

Anna V Leopold, Konstantin G Chernov, Anton A Shemetov, Vladislav V Verkhusha

Open access · goldAbstract read
In one paragraph

Article in Nature communications, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 38 papers.

0numbers the graph read from it
0cells of the map it votes in
38citing papers in PubMed
5.5field-weighted citation impact, top 3% 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

38 citing papers in PubMed, 75 citations in OpenAlex.

  1. Article
  2. Insulin Resistance and Inflammation.International journal of molecular sciences · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Opto-chemogenetic inhibition of L-type CaCell reports methods · 2024
    Article
  7. Article
  8. Fraction ofThe journal of venomous animals and toxins including tropical diseases · 2024
    Article
  9. Article
  10. Review
  11. Review
  12. Review
  13. Review
  14. Article
  15. Article
  16. Review
  17. Review
  18. Article
  19. Review
  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

4 authors at 2 institutions in 2 countries.

Anna V LeopoldMedicum, Faculty of Medicine, University of Helsinki, Helsinki, 00290, Finland.
Konstantin G ChernovMedicum, Faculty of Medicine, University of Helsinki, Helsinki, 00290, Finland.
Anton A ShemetovDepartment of Anatomy and Structural Biology, and Gruss-Lipper Biophotonics Center, Albert Einstein College of Medicine, Bronx, NY, 10461, USA.
Vladislav V VerkhushaMedicum, Faculty of Medicine, University of Helsinki, Helsinki, 00290, Finland. vladislav.verkhusha@einstein.yu.edu.
University of Helsinki · FIAlbert Einstein College of Medicine · US

Funding

Near-Infrared Fluorescent Proteins, Biosensors and Optogenetic ToolsR35GM122567 · NIGMS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI Vladislav Verkhusha · 2017 to 2026
$4.3M
Calcium biosensors for deep-tissue imaging and spectral multiplexingU01NS103573 · NINDS · ALBERT EINSTEIN COLLEGE OF MEDICINE, INC · PI VERKHUSHA, VLADISLAV · 2017 to 2019
$1.8M
NIGMS NIH HHS R35 GM122567NIH HHS GM122567NIH HHS NS103573NINDS NIH HHS U01 NS103573
6 · The paper itself

Abstract

Optical control over the activity of receptor tyrosine kinases (RTKs) provides an efficient way to reversibly and non-invasively map their functions. We combined catalytic domains of Trk (tropomyosin receptor kinase) family of RTKs, naturally activated by neurotrophins, with photosensory core module of DrBphP bacterial phytochrome to develop opto-kinases, termed Dr-TrkA and Dr-TrkB, reversibly switchable on and off with near-infrared and far-red light. We validated Dr-Trk ability to reversibly light-control several RTK pathways, calcium level, and demonstrated that their activation triggers canonical Trk signaling. Dr-TrkA induced apoptosis in neuroblastoma and glioblastoma, but not in other cell types. Absence of spectral crosstalk between Dr-Trks and blue-light-activatable LOV-domain-based translocation system enabled intracellular targeting of Dr-TrkA independently of its activation, additionally modulating Trk signaling. Dr-Trks have several superior characteristics that make them the opto-kinases of choice for regulation of RTK signaling: high activation range, fast and reversible photoswitching, and multiplexing with visible-light-controllable optogenetic tools.

Indexed as

AnimalsApoptosisBacterial ProteinsCell Line, TumorEpithelial CellsGene Expression RegulationHeLa CellsHumansInfrared RaysLight Signal TransductionMiceNerve Growth FactorsNeurogliaNeuronsOptogeneticsPhytochromeBacterial ProteinsNerve Growth FactorsPhytochromeReceptor, trkAReceptor, trkBRecombinant Fusion Proteins

Identifiers

PMID30850602
PMCPMC6408446
OpenAlexW2922439869

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.