Evidence map›Paper›PMID 26247778›Full record

ArticleJournal of the American Chemical Society2015

A Small-Molecule Photoactivatable Optical Sensor of Transmembrane Potential.

Vincent Grenier, Alison S Walker, Evan W Miller

Abstract read
In one paragraph

Article in Journal of the American Chemical Society, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing 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

20 citing papers in PubMed.

  1. Review
  2. Review
  3. Article
  4. Review
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Synthesis of Sulfonated Carbofluoresceins for Voltage Imaging.Journal of the American Chemical Society · 2019
    Article
  11. Fluorogenic Targeting of Voltage-Sensitive Dyes to Neurons.Journal of the American Chemical Society · 2017
    Article
  12. Review
  13. Article
  14. Article
  15. Exploring cells with targeted biosensors.The Journal of general physiology · 2017
    Review
  16. Article
  17. Review
  18. Isomerically Pure Tetramethylrhodamine Voltage Reporters.Journal of the American Chemical Society · 2016
    Article
  19. Article
  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

3 authors.

Vincent GrenierDepartments of †Chemistry, ‡Molecular & Cell Biology, and §Helen Wills Neuroscience Institute, University of California , Berkeley, California 94720, United States.
Alison S WalkerDepartments of †Chemistry, ‡Molecular & Cell Biology, and §Helen Wills Neuroscience Institute, University of California , Berkeley, California 94720, United States.
Evan W MillerDepartments of †Chemistry, ‡Molecular & Cell Biology, and §Helen Wills Neuroscience Institute, University of California , Berkeley, California 94720, United States.

Funding

Univ of Calif Berkeley Chemistry-Biology Interface ProgramT32GM066698 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI CHANG, CHRISTOPHER J., FRANCIS, MATTHEW B · 2004 to 2023
$7.5M
Molecular and optogenetic tools for studying voltage in the brainR00NS078561 · NINDS · UNIVERSITY OF CALIFORNIA BERKELEY · PI MILLER, EVAN WALKER · 2013 to 2015
$713k
NIGMS NIH HHS T32 GM066698NINDS NIH HHS R00 NS078561NINDS NIH HHS R00NS078561
6 · The paper itself

Abstract

This paper discloses the design, synthesis, and imaging applications of the first member of a new class of SPOTs, small-molecule photoactivatable optical sensors of transmembrane potential. SPOT2.1.Cl features an established voltage-sensitive dye, VoltageFluor2.1.Cl--or VF--capped with a dimethoxy-o-nitrobenzyl (DMNB) caging group to effectively diminish fluorescence of the VF dye prior to uncaging. SPOT2.1.Cl localizes to cell membranes and displays weak fluorescence until photoactivated. Illumination generates the parent VF dye which then optically reports on changes in the membrane voltage. After photoactivation with spatially restricted light, SPOT2.1.Cl-loaded cells display bright, voltage-sensitive fluorescence associated with the plasma membrane, while neighboring cells remain dark. Activated SPOT reports on action potentials in single trials. SPOT can be activated in neuron cell bodies or uncaged in dendrites to enable structural tracing via "backfilling" of the dye to the soma, followed by functional imaging in the labeled cell. The combination of cellular specificity achieved through spatially defined patterns of illumination, coupled with the fast, sensitive, and noncapacitive voltage sensing characteristics of VF dyes makes SPOT2.1.Cl a useful tool for interrogating both structure and function of neuronal systems.

Indexed as

Membrane PotentialsCell MembraneFluorescent DyesHEK293 CellsHumansMolecular WeightFluorescent Dyes

Identifiers

PMID26247778
PMCPMC4558294

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.