Evidence map›Paper›PMID 18601527›Full record

ArticleJournal of biomedical optics

Characterization of an improved donor fluorescent protein for Forster resonance energy transfer microscopy.

Richard N Day, Cynthia F Booker, Ammasi Periasamy

Open access · bronzeAbstract readComparative StudyEvaluation Study
In one paragraph

Article in Journal of biomedical optics. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 45 papers.

0numbers the graph read from it
0cells of the map it votes in
45citing papers in PubMed
10.7field-weighted citation impact, top 2% 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

45 citing papers in PubMed, 84 citations in OpenAlex.

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  10. Improving Quality, Reproducibility, and Usability of FRET-Based Tension Sensors.Cytometry. Part A : the journal of the International Society for Analytical Cytology · 2019
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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 at 2 institutions in 1 country.

Richard N DayUniversity of Virginia Health System, Departments of Medicine and Cell Biology, P. O. Box 800578, Charlottesville, Virginia 22908-0578, USA. rnd2v@virginia.edu
Cynthia F Booker
Ammasi Periasamy
University of Virginia Health System · USUniversity of Virginia · US

Funding

SPECIFIC REPRESSION OF PROLACTIN GENE EXPRESSIONR01DK043701 · NIDDK · UNIVERSITY OF VIRGINIA CHARLOTTESVILLE · PI DAY, RICHARD N · 1994 to 2012
$3.4M
NIDDK NIH HHS DK47301NIDDK NIH HHS R01 DK043701
6 · The paper itself

Abstract

The genetically encoded fluorescent proteins (FP), used in combination with Forster resonance energy transfer (FRET) microscopy, provide the tools necessary for the direct visualization of protein interactions inside living cells. Typically, the Cerulean and Venus variants of the cyan and yellow FPs are used for FRET studies, but there are limitations to their use. Here, Cerulean and the newly developed monomeric Teal FP (mTFP) are compared as FRET donors for Venus using spectral and fluorescence lifetime measurements from living cells. The results demonstrate that when compared to Cerulean, mTFP has increased brightness, optimal excitation using the standard 458-nm laser line, increased photostability, and improved spectral overlap with Venus. In addition, the two-photon excitation and fluorescence lifetime characteristics are determined for mTFP. Together, these measurements indicate that mTFP is an excellent donor fluorophore for FRET studies, and that its use may improve the detection of interactions involving proteins that are difficult to express, or that need to be produced at low levels in cells.

Indexed as

AnimalsCells, CulturedFluorescence Resonance Energy TransferImage EnhancementLuminescent ProteinsMiceMicroscopy, FluorescencePituitary GlandProtein Interaction MappingSensitivity and SpecificityLuminescent Proteins

Identifiers

PMID18601527
PMCPMC2483694
OpenAlexW2028176800

What OpenQuestion holds

Textmetadata
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.