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mRuby, a Bright Monomeric Red Fluorescent Protein for Labeling of Subcellular Structures
A monomeric variant of the red fluorescent protein eqFP611, mRuby, is described. With excitation and emission maxima at 558 nm and 605 nm, respectively, and a large Stokes shift of 47 nm, mRuby appears particularly useful for imaging applications. The protein shows an exceptional resistance to denat...
Autores principales: | , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2009
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633614/ https://www.ncbi.nlm.nih.gov/pubmed/19194514 http://dx.doi.org/10.1371/journal.pone.0004391 |
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author | Kredel, Simone Oswald, Franz Nienhaus, Karin Deuschle, Karen Röcker, Carlheinz Wolff, Michael Heilker, Ralf Nienhaus, G. Ulrich Wiedenmann, Jörg |
author_facet | Kredel, Simone Oswald, Franz Nienhaus, Karin Deuschle, Karen Röcker, Carlheinz Wolff, Michael Heilker, Ralf Nienhaus, G. Ulrich Wiedenmann, Jörg |
author_sort | Kredel, Simone |
collection | PubMed |
description | A monomeric variant of the red fluorescent protein eqFP611, mRuby, is described. With excitation and emission maxima at 558 nm and 605 nm, respectively, and a large Stokes shift of 47 nm, mRuby appears particularly useful for imaging applications. The protein shows an exceptional resistance to denaturation at pH extremes. Moreover, mRuby is about ten-fold brighter compared to EGFP when being targeted to the endoplasmic reticulum. The engineering process of eqFP611 revealed that the C-terminal tail of the protein acts as a natural peroxisomal targeting signal (PTS). Using an mRuby variant carrying the eqFP611-PTS, we discovered that ordered inheritance of peroxisomes is widespread during mitosis of different mammalian cell types. The ordered partitioning is realized by the formation of peroxisome clusters around the poles of the mitotic spindle and ensures that equal numbers of the organelle are inherited by the daughter cells. The unique spectral properties make mRuby the marker of choice for a multitude of cell biological applications. Moreover, the use of mRuby has allowed novel insights in the biology of organelles responsible for severe human diseases. |
format | Text |
id | pubmed-2633614 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-26336142009-02-05 mRuby, a Bright Monomeric Red Fluorescent Protein for Labeling of Subcellular Structures Kredel, Simone Oswald, Franz Nienhaus, Karin Deuschle, Karen Röcker, Carlheinz Wolff, Michael Heilker, Ralf Nienhaus, G. Ulrich Wiedenmann, Jörg PLoS One Research Article A monomeric variant of the red fluorescent protein eqFP611, mRuby, is described. With excitation and emission maxima at 558 nm and 605 nm, respectively, and a large Stokes shift of 47 nm, mRuby appears particularly useful for imaging applications. The protein shows an exceptional resistance to denaturation at pH extremes. Moreover, mRuby is about ten-fold brighter compared to EGFP when being targeted to the endoplasmic reticulum. The engineering process of eqFP611 revealed that the C-terminal tail of the protein acts as a natural peroxisomal targeting signal (PTS). Using an mRuby variant carrying the eqFP611-PTS, we discovered that ordered inheritance of peroxisomes is widespread during mitosis of different mammalian cell types. The ordered partitioning is realized by the formation of peroxisome clusters around the poles of the mitotic spindle and ensures that equal numbers of the organelle are inherited by the daughter cells. The unique spectral properties make mRuby the marker of choice for a multitude of cell biological applications. Moreover, the use of mRuby has allowed novel insights in the biology of organelles responsible for severe human diseases. Public Library of Science 2009-02-05 /pmc/articles/PMC2633614/ /pubmed/19194514 http://dx.doi.org/10.1371/journal.pone.0004391 Text en Kredel et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Kredel, Simone Oswald, Franz Nienhaus, Karin Deuschle, Karen Röcker, Carlheinz Wolff, Michael Heilker, Ralf Nienhaus, G. Ulrich Wiedenmann, Jörg mRuby, a Bright Monomeric Red Fluorescent Protein for Labeling of Subcellular Structures |
title | mRuby, a Bright Monomeric Red Fluorescent Protein for Labeling of Subcellular Structures |
title_full | mRuby, a Bright Monomeric Red Fluorescent Protein for Labeling of Subcellular Structures |
title_fullStr | mRuby, a Bright Monomeric Red Fluorescent Protein for Labeling of Subcellular Structures |
title_full_unstemmed | mRuby, a Bright Monomeric Red Fluorescent Protein for Labeling of Subcellular Structures |
title_short | mRuby, a Bright Monomeric Red Fluorescent Protein for Labeling of Subcellular Structures |
title_sort | mruby, a bright monomeric red fluorescent protein for labeling of subcellular structures |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2633614/ https://www.ncbi.nlm.nih.gov/pubmed/19194514 http://dx.doi.org/10.1371/journal.pone.0004391 |
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