Evidence map›Paper›PMID 24099419›Full record

ArticleJournal of the American Chemical Society2013

Optically modulatable blue fluorescent proteins.

Amy E Jablonski, Russell B Vegh, Jung-Cheng Hsiang, Bettina Bommarius, Yen-Cheng Chen, Kyril M Solntsev, Andreas S Bommarius, Laren M Tolbert, Robert M Dickson

Open access · greenAbstract 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 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
6.7field-weighted citation impact, top 4% 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

14 citing papers in PubMed, 37 citations in OpenAlex.

  1. Review of FRET biosensing and its application in biomolecular detection.American journal of translational research · 2023
    Review
  2. Chromophore reduction plus reversible photobleaching: how the mKate2 "photoconversion" works.Photochemical & photobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology · 2021
    Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Optically Activated Delayed Fluorescence.The journal of physical chemistry letters · 2017
    Article
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  10. Article
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  12. Article
  13. Review
  14. 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

9 authors at 1 institution in 1 country.

Amy E JablonskiSchool of Chemistry and Biochemistry, ‡School of Chemical and Biomolecular Engineering, and §Petit Institute for Bioengineering and Bioscience, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.
Russell B Vegh
Jung-Cheng Hsiang
Bettina Bommarius
Yen-Cheng Chen
Kyril M Solntsev
Andreas S Bommarius
Laren M Tolbert
Robert M Dickson
Georgia Institute of Technology · US

Funding

Optically Modulated Fluorescent ProteinsR21EB009976 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI DICKSON, ROBERT M, TOLBERT, LAREN MALCOLM · 2009 to 2010
$398k
NIBIB NIH HHS R21 EB009976NIBIB NIH HHS R21EB009976
6 · The paper itself

Abstract

Blue fluorescent proteins (BFPs) offer visualization of protein location and behavior, but often suffer from high autofluorescent background and poor signal discrimination. Through dual-laser excitation of bright and photoinduced dark states, mutations to the residues surrounding the BFP chromophore enable long-wavelength optical modulation of BFP emission. Such dark state engineering enables violet-excited blue emission to be increased upon lower energy, green coillumination. Turning this green coillumination on and off at a specific frequency dynamically modulates collected blue fluorescence without generating additional background. Interpreted as transient photoconversion between neutral cis and anionic trans chromophoric forms, mutations tune photoisomerization and ground state tautomerizations to enable long-wavelength depopulation of the millisecond-lived, spectrally shifted dark states. Single mutations to the tyrosine-based blue fluorescent protein T203V/S205V exhibit enhanced modulation depth and varied frequency. Importantly, analogous single point mutations in the nonmodulatable BFP, mKalama1, creates a modulatable variant. Building modulatable BFPs offers opportunities for improved BFP signal discrimination vs background, greatly enhancing their utility.

Indexed as

AnimalsCells, CulturedLuminescent ProteinsMiceMicroscopy, FluorescenceModels, MolecularMutagenesis, Site-DirectedNIH 3T3 CellsOptical PhenomenaLuminescent Proteins

Identifiers

PMID24099419
PMCPMC3885243
OpenAlexW1972509634

What OpenQuestion holds

Textmetadata
LicenceTDM
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.