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eZinCh-2: A Versatile, Genetically Encoded FRET Sensor for Cytosolic and Intraorganelle Zn(2+) Imaging
[Image: see text] Zn(2+) plays essential and diverse roles in numerous cellular processes. To get a better understanding of intracellular Zn(2+) homeostasis and the putative signaling role of Zn(2+), various fluorescent sensors have been developed that allow monitoring of Zn(2+) concentrations in si...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical
Society
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577962/ https://www.ncbi.nlm.nih.gov/pubmed/26151333 http://dx.doi.org/10.1021/acschembio.5b00211 |
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author | Hessels, Anne M. Chabosseau, Pauline Bakker, Maarten H. Engelen, Wouter Rutter, Guy A. Taylor, Kathryn M. Merkx, Maarten |
author_facet | Hessels, Anne M. Chabosseau, Pauline Bakker, Maarten H. Engelen, Wouter Rutter, Guy A. Taylor, Kathryn M. Merkx, Maarten |
author_sort | Hessels, Anne M. |
collection | PubMed |
description | [Image: see text] Zn(2+) plays essential and diverse roles in numerous cellular processes. To get a better understanding of intracellular Zn(2+) homeostasis and the putative signaling role of Zn(2+), various fluorescent sensors have been developed that allow monitoring of Zn(2+) concentrations in single living cells in real time. Thus far, two families of genetically encoded FRET-based Zn(2+) sensors have been most widely applied, the eCALWY sensors developed by our group and the ZapCY sensors developed by Palmer and co-workers. Both have been successfully used to measure cytosolic free Zn(2+), but distinctly different concentrations have been reported when using these sensors to measure Zn(2+) concentrations in the ER and mitochondria. Here, we report the development of a versatile alternative FRET sensor containing a de novo Cys(2)His(2) binding pocket that was created on the surface of the donor and acceptor fluorescent domains. This eZinCh-2 sensor binds Zn(2+) with a high affinity that is similar to that of eCALWY-4 (K(d) = 1 nM at pH 7.1), while displaying a substantially larger change in emission ratio. eZinCh-2 not only provides an attractive alternative for measuring Zn(2+) in the cytosol but was also successfully used for measuring Zn(2+) in the ER, mitochondria, and secretory vesicles. Moreover, organelle-targeted eZinCh-2 can also be used in combination with the previously reported redCALWY sensors to allow multicolor imaging of intracellular Zn(2+) simultaneously in the cytosol and the ER or mitochondria. |
format | Online Article Text |
id | pubmed-4577962 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | American Chemical
Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-45779622015-09-30 eZinCh-2: A Versatile, Genetically Encoded FRET Sensor for Cytosolic and Intraorganelle Zn(2+) Imaging Hessels, Anne M. Chabosseau, Pauline Bakker, Maarten H. Engelen, Wouter Rutter, Guy A. Taylor, Kathryn M. Merkx, Maarten ACS Chem Biol [Image: see text] Zn(2+) plays essential and diverse roles in numerous cellular processes. To get a better understanding of intracellular Zn(2+) homeostasis and the putative signaling role of Zn(2+), various fluorescent sensors have been developed that allow monitoring of Zn(2+) concentrations in single living cells in real time. Thus far, two families of genetically encoded FRET-based Zn(2+) sensors have been most widely applied, the eCALWY sensors developed by our group and the ZapCY sensors developed by Palmer and co-workers. Both have been successfully used to measure cytosolic free Zn(2+), but distinctly different concentrations have been reported when using these sensors to measure Zn(2+) concentrations in the ER and mitochondria. Here, we report the development of a versatile alternative FRET sensor containing a de novo Cys(2)His(2) binding pocket that was created on the surface of the donor and acceptor fluorescent domains. This eZinCh-2 sensor binds Zn(2+) with a high affinity that is similar to that of eCALWY-4 (K(d) = 1 nM at pH 7.1), while displaying a substantially larger change in emission ratio. eZinCh-2 not only provides an attractive alternative for measuring Zn(2+) in the cytosol but was also successfully used for measuring Zn(2+) in the ER, mitochondria, and secretory vesicles. Moreover, organelle-targeted eZinCh-2 can also be used in combination with the previously reported redCALWY sensors to allow multicolor imaging of intracellular Zn(2+) simultaneously in the cytosol and the ER or mitochondria. American Chemical Society 2015-07-07 2015-09-18 /pmc/articles/PMC4577962/ /pubmed/26151333 http://dx.doi.org/10.1021/acschembio.5b00211 Text en Copyright © 2015 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Hessels, Anne M. Chabosseau, Pauline Bakker, Maarten H. Engelen, Wouter Rutter, Guy A. Taylor, Kathryn M. Merkx, Maarten eZinCh-2: A Versatile, Genetically Encoded FRET Sensor for Cytosolic and Intraorganelle Zn(2+) Imaging |
title | eZinCh-2: A Versatile, Genetically Encoded FRET Sensor
for Cytosolic and Intraorganelle Zn(2+) Imaging |
title_full | eZinCh-2: A Versatile, Genetically Encoded FRET Sensor
for Cytosolic and Intraorganelle Zn(2+) Imaging |
title_fullStr | eZinCh-2: A Versatile, Genetically Encoded FRET Sensor
for Cytosolic and Intraorganelle Zn(2+) Imaging |
title_full_unstemmed | eZinCh-2: A Versatile, Genetically Encoded FRET Sensor
for Cytosolic and Intraorganelle Zn(2+) Imaging |
title_short | eZinCh-2: A Versatile, Genetically Encoded FRET Sensor
for Cytosolic and Intraorganelle Zn(2+) Imaging |
title_sort | ezinch-2: a versatile, genetically encoded fret sensor
for cytosolic and intraorganelle zn(2+) imaging |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4577962/ https://www.ncbi.nlm.nih.gov/pubmed/26151333 http://dx.doi.org/10.1021/acschembio.5b00211 |
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