Evidence map›Paper›PMID 25536421›Full record

ArticlePloS one2014

Interfacial polymerization for colorimetric labeling of protein expression in cells.

Jacob L Lilly, Phillip R Sheldon, Liv J Hoversten, Gabriela Romero, Vivek Balasubramaniam, Brad J Berron

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.0field-weighted citation impact, top 25% 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

3 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

6 authors at 2 institutions in 1 country.

Jacob L LillyDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, Kentucky, United States of America.
Phillip R SheldonDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, Kentucky, United States of America.
Liv J HoverstenDepartment of Pediatrics, University of Colorado, Denver, Colorado, United States of America.
Gabriela RomeroDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, Kentucky, United States of America.
Vivek BalasubramaniamDepartment of Pediatrics, University of Colorado, Denver, Colorado, United States of America.
Brad J BerronDepartment of Chemical and Materials Engineering, University of Kentucky, Lexington, Kentucky, United States of America.
University of Kentucky · USUniversity of Colorado Denver · US

Funding

The University of Kentucky Cancer Nanotechnology Training Center (UK CNTC)R25CA153954 · NCI · UNIVERSITY OF KENTUCKY · PI ANDERSON, BRADLEY D, EVERS, BERNARD MARK · 2010 to 2014
$1.6M
Collaboration in the Development of Novel Polymerization Enhanced ImmunofluoresceR21EB012188 · NIBIB · UNIVERSITY OF COLORADO · PI BOWMAN, CHRISTOPHER N · 2011 to 2012
$413k
NCI NIH HHS R25 CA153954NCI NIH HHS R25CA153954NIBIB NIH HHS R21 EB012188
6 · The paper itself

Abstract

Determining the location of rare proteins in cells typically requires the use of on-sample amplification. Antibody based recognition and enzymatic amplification is used to produce large amounts of visible label at the site of protein expression, but these techniques suffer from the presence of nonspecific reactivity in the biological sample and from poor spatial control over the label. Polymerization based amplification is a recently developed alternative means of creating an on-sample amplification for fluorescence applications, while not suffering from endogenous labels or loss of signal localization. This manuscript builds upon polymerization based amplification by developing a stable, archivable, and colorimetric mode of amplification termed Polymer Dye Labeling. The basic concept involves an interfacial polymer grown at the site of protein expression and subsequent staining of this polymer with an appropriate dye. The dyes Evans Blue and eosin were initially investigated for colorimetric response in a microarray setting, where both specifically stained polymer films on glass. The process was translated to the staining of protein expression in human dermal fibroblast cells, and Polymer Dye Labeling was specific to regions consistent with desired protein expression. The labeling is stable for over 200 days in ambient conditions and is also compatible with modern mounting medium.

Indexed as

ColorimetryColoring AgentsEosine Yellowish-(YS)Evans BlueFibroblastsHumansPolymerizationProteinsStaining and LabelingColoring AgentsEosine Yellowish-(YS)Evans BlueProteins

Identifiers

PMID25536421
PMCPMC4275217
OpenAlexW2049190998

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.