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Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag
The use of fluorescent and luminescent proteins in visualizing proteins has become a powerful tool in understanding molecular and cellular processes within living organisms. This success has resulted in an ever-increasing demand for new and more versatile protein-labeling tools that permit light-bas...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Society for Microbiology
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800872/ https://www.ncbi.nlm.nih.gov/pubmed/26787765 http://dx.doi.org/10.1128/JB.00864-15 |
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author | Ke, Na Landgraf, Dirk Paulsson, Johan Berkmen, Mehmet |
author_facet | Ke, Na Landgraf, Dirk Paulsson, Johan Berkmen, Mehmet |
author_sort | Ke, Na |
collection | PubMed |
description | The use of fluorescent and luminescent proteins in visualizing proteins has become a powerful tool in understanding molecular and cellular processes within living organisms. This success has resulted in an ever-increasing demand for new and more versatile protein-labeling tools that permit light-based detection of proteins within living cells. In this report, we present data supporting the use of the self-labeling HaloTag protein as a light-emitting reporter for protein fusions within the model prokaryote Escherichia coli. We show that functional protein fusions of the HaloTag can be detected both in vivo and in vitro when expressed within the cytoplasmic or periplasmic compartments of E. coli. The capacity to visually detect proteins localized in various prokaryotic compartments expands today's molecular biologist toolbox and paves the path to new applications. IMPORTANCE Visualizing proteins microscopically within living cells is important for understanding both the biology of cells and the role of proteins within living cells. Currently, the most common tool is green fluorescent protein (GFP). However, fluorescent proteins such as GFP have many limitations; therefore, the field of molecular biology is always in need of new tools to visualize proteins. In this paper, we demonstrate, for the first time, the use of HaloTag to visualize proteins in two different compartments within the model prokaryote Escherichia coli. The use of HaloTag as an additional tool to visualize proteins within prokaryotes increases our capacity to ask about and understand the role of proteins within living cells. |
format | Online Article Text |
id | pubmed-4800872 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | American Society for Microbiology |
record_format | MEDLINE/PubMed |
spelling | pubmed-48008722016-04-04 Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag Ke, Na Landgraf, Dirk Paulsson, Johan Berkmen, Mehmet J Bacteriol Articles The use of fluorescent and luminescent proteins in visualizing proteins has become a powerful tool in understanding molecular and cellular processes within living organisms. This success has resulted in an ever-increasing demand for new and more versatile protein-labeling tools that permit light-based detection of proteins within living cells. In this report, we present data supporting the use of the self-labeling HaloTag protein as a light-emitting reporter for protein fusions within the model prokaryote Escherichia coli. We show that functional protein fusions of the HaloTag can be detected both in vivo and in vitro when expressed within the cytoplasmic or periplasmic compartments of E. coli. The capacity to visually detect proteins localized in various prokaryotic compartments expands today's molecular biologist toolbox and paves the path to new applications. IMPORTANCE Visualizing proteins microscopically within living cells is important for understanding both the biology of cells and the role of proteins within living cells. Currently, the most common tool is green fluorescent protein (GFP). However, fluorescent proteins such as GFP have many limitations; therefore, the field of molecular biology is always in need of new tools to visualize proteins. In this paper, we demonstrate, for the first time, the use of HaloTag to visualize proteins in two different compartments within the model prokaryote Escherichia coli. The use of HaloTag as an additional tool to visualize proteins within prokaryotes increases our capacity to ask about and understand the role of proteins within living cells. American Society for Microbiology 2016-03-17 /pmc/articles/PMC4800872/ /pubmed/26787765 http://dx.doi.org/10.1128/JB.00864-15 Text en Copyright © 2016 Ke et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license (http://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Articles Ke, Na Landgraf, Dirk Paulsson, Johan Berkmen, Mehmet Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag |
title | Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag |
title_full | Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag |
title_fullStr | Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag |
title_full_unstemmed | Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag |
title_short | Visualization of Periplasmic and Cytoplasmic Proteins with a Self-Labeling Protein Tag |
title_sort | visualization of periplasmic and cytoplasmic proteins with a self-labeling protein tag |
topic | Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4800872/ https://www.ncbi.nlm.nih.gov/pubmed/26787765 http://dx.doi.org/10.1128/JB.00864-15 |
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