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Protein Expression Analyses at the Single Cell Level

The central dogma of molecular biology explains how genetic information is converted into its end product, proteins, which are responsible for the phenotypic state of the cell. Along with the protein type, the phenotypic state depends on the protein copy number. Therefore, quantification of the prot...

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Detalles Bibliográficos
Autores principales: Ohno, Masae, Karagiannis, Peter, Taniguchi, Yuichi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270791/
https://www.ncbi.nlm.nih.gov/pubmed/25197931
http://dx.doi.org/10.3390/molecules190913932
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author Ohno, Masae
Karagiannis, Peter
Taniguchi, Yuichi
author_facet Ohno, Masae
Karagiannis, Peter
Taniguchi, Yuichi
author_sort Ohno, Masae
collection PubMed
description The central dogma of molecular biology explains how genetic information is converted into its end product, proteins, which are responsible for the phenotypic state of the cell. Along with the protein type, the phenotypic state depends on the protein copy number. Therefore, quantification of the protein expression in a single cell is critical for quantitative characterization of the phenotypic states. Protein expression is typically a dynamic and stochastic phenomenon that cannot be well described by standard experimental methods. As an alternative, fluorescence imaging is being explored for the study of protein expression, because of its high sensitivity and high throughput. Here we review key recent progresses in fluorescence imaging-based methods and discuss their application to proteome analysis at the single cell level.
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spelling pubmed-62707912018-12-27 Protein Expression Analyses at the Single Cell Level Ohno, Masae Karagiannis, Peter Taniguchi, Yuichi Molecules Review The central dogma of molecular biology explains how genetic information is converted into its end product, proteins, which are responsible for the phenotypic state of the cell. Along with the protein type, the phenotypic state depends on the protein copy number. Therefore, quantification of the protein expression in a single cell is critical for quantitative characterization of the phenotypic states. Protein expression is typically a dynamic and stochastic phenomenon that cannot be well described by standard experimental methods. As an alternative, fluorescence imaging is being explored for the study of protein expression, because of its high sensitivity and high throughput. Here we review key recent progresses in fluorescence imaging-based methods and discuss their application to proteome analysis at the single cell level. MDPI 2014-09-05 /pmc/articles/PMC6270791/ /pubmed/25197931 http://dx.doi.org/10.3390/molecules190913932 Text en © 2014 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/3.0/).
spellingShingle Review
Ohno, Masae
Karagiannis, Peter
Taniguchi, Yuichi
Protein Expression Analyses at the Single Cell Level
title Protein Expression Analyses at the Single Cell Level
title_full Protein Expression Analyses at the Single Cell Level
title_fullStr Protein Expression Analyses at the Single Cell Level
title_full_unstemmed Protein Expression Analyses at the Single Cell Level
title_short Protein Expression Analyses at the Single Cell Level
title_sort protein expression analyses at the single cell level
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6270791/
https://www.ncbi.nlm.nih.gov/pubmed/25197931
http://dx.doi.org/10.3390/molecules190913932
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