Evidence map›Paper›PMID 27159569›Full record

ArticleBioconjugate chemistry2016

Multiexcitation Fluorogenic Labeling of Surface, Intracellular, and Total Protein Pools in Living Cells.

Matharishwan Naganbabu, Lydia A Perkins, Yi Wang, Jeffery Kurish, Brigitte F Schmidt, Marcel P Bruchez

Open access · bronzeAbstract read
In one paragraph

Article in Bioconjugate chemistry, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.5field-weighted citation impact, top 20% 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

9 citing papers in PubMed, 16 citations in OpenAlex.

  1. Reversible, Chemically Gated FRET via Ligand-Activated Acceptors.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026
    Article
  2. Article
  3. Article
  4. Interrogating surfaceChemical science · 2020
    Article
  5. Article
  6. Review
  7. Review
  8. Article
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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

6 authors at 2 institutions in 1 country.

Matharishwan NaganbabuDepartment of Chemistry, ‡Department of Biological Sciences, and §Molecular Biosensors and Imaging Center, Carnegie Mellon University , 4400 Fifth Avenue, Pittsburgh 15213, Pennsylvania, United States.
Lydia A PerkinsDepartment of Chemistry, ‡Department of Biological Sciences, and §Molecular Biosensors and Imaging Center, Carnegie Mellon University , 4400 Fifth Avenue, Pittsburgh 15213, Pennsylvania, United States.
Yi WangDepartment of Chemistry, ‡Department of Biological Sciences, and §Molecular Biosensors and Imaging Center, Carnegie Mellon University , 4400 Fifth Avenue, Pittsburgh 15213, Pennsylvania, United States.
Jeffery KurishDepartment of Chemistry, ‡Department of Biological Sciences, and §Molecular Biosensors and Imaging Center, Carnegie Mellon University , 4400 Fifth Avenue, Pittsburgh 15213, Pennsylvania, United States.
Brigitte F SchmidtDepartment of Chemistry, ‡Department of Biological Sciences, and §Molecular Biosensors and Imaging Center, Carnegie Mellon University , 4400 Fifth Avenue, Pittsburgh 15213, Pennsylvania, United States.
Marcel P BruchezDepartment of Chemistry, ‡Department of Biological Sciences, and §Molecular Biosensors and Imaging Center, Carnegie Mellon University , 4400 Fifth Avenue, Pittsburgh 15213, Pennsylvania, United States.
Carnegie Mellon University · USImaging Center · US

Funding

Targeted fluorescent indicators for endothelial physiology: Ca(II), ROS, NOR01EB017268 · NIBIB · CARNEGIE-MELLON UNIVERSITY · PI BRUCHEZ, MARCEL P, ST CROIX, CLAUDETTE MARIE · 2013 to 2016
$2.5M
NIBIB NIH HHS R01 EB017268
6 · The paper itself

Abstract

Malachite green (MG) is a fluorogenic dye that shows fluorescence enhancement upon binding to its engineered cognate protein, a fluorogen activating protein (FAP). Energy transfer donors such as cyanine and rhodamine dyes have been conjugated with MG to modify the spectral properties of the fluorescent complexes, where the donor dyes transfer energy through Förster resonance energy transfer to the MG complex resulting in binding-conditional fluorescence emission in the far-red region. In this article, we use a violet-excitable dye as a donor to sensitize the far-red emission of the MG-FAP complex. Two blue emitting fluorescent coumarin dyes were coupled to MG and evaluated for energy transfer to the MG-FAP complex via its secondary excitation band. 6,8-Difluoro-7-hydroxycoumarin-3-carboxylic acid (Pacific blue, PB) showed the most efficient energy transfer and maximum brightness in the far-red region upon violet (405 nm) excitation. These blue-red (BluR) tandem dyes are spectrally varied from other tandem dyes and are able to produce fluorescence images of the MG-FAP complex with a large Stokes shift (>250 nm). These dyes are cell-permeable and are used to label intracellular proteins. Used together with a cell-impermeable hexa-Cy3-MG (HCM) dye that labels extracellular proteins, we are able to visualize extracellular, intracellular, and total pools of cellular protein using one fluorogenic tag that combines with distinct dyes to effect different spectral characteristics.

Indexed as

Cell SurvivalFluorescent DyesHEK293 CellsHumansIntracellular SpaceProteinsRosaniline DyesSurface PropertiesFluorescent Dyesmalachite greenProteinsRosaniline Dyes

Identifiers

PMID27159569
PMCPMC4911959
OpenAlexW2347009463

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.