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A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling†
[Image: see text] Fluorescent proteins (FPs) with far-red excitation and emission are desirable for multicolor labeling and live-animal imaging. We describe E2-Crimson, a far-red derivative of the tetrameric FP DsRed-Express2. Unlike other far-red FPs, E2-Crimson is noncytotoxic in bacterial and mam...
Autores principales: | , , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2009
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861903/ https://www.ncbi.nlm.nih.gov/pubmed/19658435 http://dx.doi.org/10.1021/bi900870u |
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author | Strack, Rita L. Hein, Birka Bhattacharyya, Dibyendu Hell, Stefan W. Keenan, Robert J. Glick, Benjamin S. |
author_facet | Strack, Rita L. Hein, Birka Bhattacharyya, Dibyendu Hell, Stefan W. Keenan, Robert J. Glick, Benjamin S. |
author_sort | Strack, Rita L. |
collection | PubMed |
description | [Image: see text] Fluorescent proteins (FPs) with far-red excitation and emission are desirable for multicolor labeling and live-animal imaging. We describe E2-Crimson, a far-red derivative of the tetrameric FP DsRed-Express2. Unlike other far-red FPs, E2-Crimson is noncytotoxic in bacterial and mammalian cells. E2-Crimson is brighter than other far-red FPs and matures substantially faster than other red and far-red FPs. Approximately 40% of the E2-Crimson fluorescence signal is remarkably photostable. With an excitation maximum at 611 nm, E2-Crimson is the first FP that is efficiently excited with standard far-red lasers. We show that E2-Crimson has unique applications for flow cytometry and stimulated emission depletion (STED) microscopy. |
format | Text |
id | pubmed-2861903 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2009 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-28619032010-04-30 A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling† Strack, Rita L. Hein, Birka Bhattacharyya, Dibyendu Hell, Stefan W. Keenan, Robert J. Glick, Benjamin S. Biochemistry [Image: see text] Fluorescent proteins (FPs) with far-red excitation and emission are desirable for multicolor labeling and live-animal imaging. We describe E2-Crimson, a far-red derivative of the tetrameric FP DsRed-Express2. Unlike other far-red FPs, E2-Crimson is noncytotoxic in bacterial and mammalian cells. E2-Crimson is brighter than other far-red FPs and matures substantially faster than other red and far-red FPs. Approximately 40% of the E2-Crimson fluorescence signal is remarkably photostable. With an excitation maximum at 611 nm, E2-Crimson is the first FP that is efficiently excited with standard far-red lasers. We show that E2-Crimson has unique applications for flow cytometry and stimulated emission depletion (STED) microscopy. American Chemical Society 2009-08-06 2009-09-08 /pmc/articles/PMC2861903/ /pubmed/19658435 http://dx.doi.org/10.1021/bi900870u Text en Copyright © 2009 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Strack, Rita L. Hein, Birka Bhattacharyya, Dibyendu Hell, Stefan W. Keenan, Robert J. Glick, Benjamin S. A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling† |
title | A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling† |
title_full | A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling† |
title_fullStr | A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling† |
title_full_unstemmed | A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling† |
title_short | A Rapidly Maturing Far-Red Derivative of DsRed-Express2 for Whole-Cell Labeling† |
title_sort | rapidly maturing far-red derivative of dsred-express2 for whole-cell labeling† |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861903/ https://www.ncbi.nlm.nih.gov/pubmed/19658435 http://dx.doi.org/10.1021/bi900870u |
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