Evidence map›Paper›PMID 24117060›Full record

ArticleJournal of the American Chemical Society2013

Spectral evolution of a photochemical protecting group for orthogonal two-color uncaging with visible light.

Jeremy P Olson, Matthew R Banghart, Bernardo L Sabatini, Graham C R Ellis-Davies

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing 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

39 citing papers in PubMed.

  1. Review
  2. Photocleavable Systems for Cell Biology: Conceptual Design across Molecular Modalities.Chembiochem : a European journal of chemical biology · 2025
    Review
  3. Synthesis and characterization of coumarin-derived sulfur analogues using Lawesson's reagent.Acta crystallographica. Section C, Structural chemistry · 2025
    Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Neural and behavioral control inProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  14. Light-Controlled Cell-Cycle Arrest and Apoptosis.Angewandte Chemie (International ed. in English) · 2021
    Article
  15. Article
  16. Article
  17. Conditionally Activatable Visible-Light Photocages.Journal of the American Chemical Society · 2020
    Article
  18. Article
  19. Useful Caged Compounds for Cell Physiology.Accounts of chemical research · 2020
    Article
  20. Water-Soluble BODIPY Photocages with Tunable Cellular Localization.Journal of the American Chemical Society · 2020
    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.

Jeremy P OlsonDepartment of Neuroscience, Mount Sinai School of Medicine , New York, New York 10029, United States.
Matthew R Banghart
Bernardo L Sabatini
Graham C R Ellis-Davies

Funding

PHOTOCHEMICAL REGULATION OF CALCIUM IN CELL PHYSIOLOGYR01GM053395 · NIGMS · OREGON HEALTH AND SCIENCE UNIVERSITY · PI ELLIS-DAVIES, GRAHAM · 1995 to 2020
$6.1M
Optical probes for controlling cellular functionR01NS069720 · NINDS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI ELLIS-DAVIES, GRAHAM · 2010 to 2017
$3.2M
Regulation of neuron and synapse function by neuropeptidesR01MH085498 · NIMH · HARVARD MEDICAL SCHOOL · PI SABATINI, BERNARDO L · 2008 to 2011
$1.3M
Compartment-Specific Signaling Of Striatal Opioid Peptides in Reward-Guided BehavK99DA034648 · NIDA · HARVARD MEDICAL SCHOOL · PI BANGHART, MATTHEW R. · 2013 to 2014
$243k
Howard Hughes Medical InstituteNIDA NIH HHS K99 DA034648NIGMS NIH HHS GM053395NIGMS NIH HHS R01 GM053395NIMH NIH HHS MH085498NIMH NIH HHS R01 MH085498NINDS NIH HHS NS069720NINDS NIH HHS R01 NS069720
6 · The paper itself

Abstract

Caged compounds are molecules rendered functionally inert by derivatization with a photochemical protecting group. We describe the design logic behind the development of a diethylaminocoumarin (DEAC) caging chromophore, DEAC450, that absorbs blue light strongly (ε450 = 43,000 M(-1) cm(-1)) and violet light 11-fold more weakly. The absorption minimum is in the wavelength range (340-360 nm) that is traditionally used for photolysis of many widely used nitroaromatic caged compounds (e.g., 4-carboxymethoxy-5,7-dinitroindolinyl(CDNI)-GABA). We used this chromophore to synthesize DEAC450-caged cAMP and found this probe was very stable toward aqueous hydrolysis in the electronic ground state but was photolyzed with a quantum efficiency of 0.78. When DEAC450-cAMP and CDNI-GABA where co-applied to striatal cholinergic interneurons, the caged compounds were photolyzed in an chromatically orthogonal manner using blue and violet light so as to modulate the neuronal firing rate in a bidirectional way.

Indexed as

ColorLightAminocoumarinsCoumarinsCyclic AMPgamma-Aminobutyric AcidHydrolysisMolecular StructurePhotochemical ProcessesAminocoumarinsCoumarinsCyclic AMPgamma-Aminobutyric Acid

Identifiers

PMID24117060
PMCPMC4097017

What OpenQuestion holds

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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.