Interfacial polymerization for colorimetric labeling of protein expression in cells.

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 nonsp...

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Main Authors: Jacob L Lilly, Phillip R Sheldon, Liv J Hoversten, Gabriela Romero, Vivek Balasubramaniam, Brad J Berron
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4275217?pdf=render
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spelling doaj-8a2841ff216e43e391ba4bacdfb1c79d2020-11-24T21:35:12ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-01912e11563010.1371/journal.pone.0115630Interfacial polymerization for colorimetric labeling of protein expression in cells.Jacob L LillyPhillip R SheldonLiv J HoverstenGabriela RomeroVivek BalasubramaniamBrad J BerronDetermining 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.http://europepmc.org/articles/PMC4275217?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Jacob L Lilly
Phillip R Sheldon
Liv J Hoversten
Gabriela Romero
Vivek Balasubramaniam
Brad J Berron
spellingShingle Jacob L Lilly
Phillip R Sheldon
Liv J Hoversten
Gabriela Romero
Vivek Balasubramaniam
Brad J Berron
Interfacial polymerization for colorimetric labeling of protein expression in cells.
PLoS ONE
author_facet Jacob L Lilly
Phillip R Sheldon
Liv J Hoversten
Gabriela Romero
Vivek Balasubramaniam
Brad J Berron
author_sort Jacob L Lilly
title Interfacial polymerization for colorimetric labeling of protein expression in cells.
title_short Interfacial polymerization for colorimetric labeling of protein expression in cells.
title_full Interfacial polymerization for colorimetric labeling of protein expression in cells.
title_fullStr Interfacial polymerization for colorimetric labeling of protein expression in cells.
title_full_unstemmed Interfacial polymerization for colorimetric labeling of protein expression in cells.
title_sort interfacial polymerization for colorimetric labeling of protein expression in cells.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description 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.
url http://europepmc.org/articles/PMC4275217?pdf=render
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