Evidence map›Paper›PMID 26402244›Full record

ArticleJournal of the American Chemical Society2015

Optically Modulated Photoswitchable Fluorescent Proteins Yield Improved Biological Imaging Sensitivity.

Yen-Cheng Chen, Amy E Jablonski, Irina Issaeva, Daisy Bourassa, Jung-Cheng Hsiang, Christoph J Fahrni, Robert M Dickson

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 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

10 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Photoswitchable Fluorescent Proteins: Mechanisms on Ultrafast Timescales.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Article
  9. Optically Activated Delayed Fluorescence.The journal of physical chemistry letters · 2017
    Article
  10. 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

7 authors.

Yen-Cheng ChenSchool of Chemistry and Biochemistry and Petit Institute for Bioscience and Bioengineering, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.
Amy E JablonskiSchool of Chemistry and Biochemistry and Petit Institute for Bioscience and Bioengineering, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.
Irina IssaevaSchool of Chemistry and Biochemistry and Petit Institute for Bioscience and Bioengineering, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.
Daisy BourassaSchool of Chemistry and Biochemistry and Petit Institute for Bioscience and Bioengineering, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.
Jung-Cheng HsiangSchool of Chemistry and Biochemistry and Petit Institute for Bioscience and Bioengineering, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.
Christoph J FahrniSchool of Chemistry and Biochemistry and Petit Institute for Bioscience and Bioengineering, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.
Robert M DicksonSchool of Chemistry and Biochemistry and Petit Institute for Bioscience and Bioengineering, Georgia Institute of Technology , Atlanta, Georgia 30332-0400, United States.

Funding

Expanded dimensionality and high sensitivity cell imaging using designed OMFPsR21EB020371 · NIBIB · GEORGIA INSTITUTE OF TECHNOLOGY · PI DICKSON, ROBERT M · 2015 to 2016
$401k
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 R21EB009976NIBIB NIH HHS R21 EB020371NIBIB NIH HHS R21EB020371
6 · The paper itself

Abstract

Photoswitchable fluorescent proteins (PS-FPs) open grand new opportunities in biological imaging. Through optical manipulation of FP emission, we demonstrate that dual-laser modulated synchronously amplified fluorescence image recovery (DM-SAFIRe) improves signal contrast in high background through unambiguous demodulation and is linear in relative fluorophore abundance at different points in the cell. The unique bright-to-dark state interconversion rates of each PS-FP not only enables discrimination of different, yet spectrally indistinguishable FPs, but also allows signal rejection of diffusing relative to bound forms of the same PS-FP, rsFastLime. Adding to the sensitivity gains realized from rejecting non-modulatable background, the selective signal recovery of immobilized vs diffusing intracellular rsFastLime suggests that DM-SAFIRe can detect weak protein-protein interactions that are normally obscured by large fractions of unbound FPs.

Indexed as

Eye ProteinsLuminescent ProteinsEye ProteinsLuminescent Proteins

Identifiers

PMID26402244
PMCPMC4876716

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.