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Protocol for Quantifying Zinc Flux in Cultured Cells using Fluorescent Indicators

Zinc (Zn(2+)) plays a vital role in the functioning of the cell. Cells have influx and efflux zinc transporters to regulate the levels of Zn(2+) in the cytoplasm and organellar compartments to maintain homeostasis. We present a protocol to measure changes in cellular zinc concentrations using either...

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Detalles Bibliográficos
Autores principales: Ali, Saima, Cuajungco, Math P.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580219/
https://www.ncbi.nlm.nih.gov/pubmed/33111096
http://dx.doi.org/10.1016/j.xpro.2020.100050
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author Ali, Saima
Cuajungco, Math P.
author_facet Ali, Saima
Cuajungco, Math P.
author_sort Ali, Saima
collection PubMed
description Zinc (Zn(2+)) plays a vital role in the functioning of the cell. Cells have influx and efflux zinc transporters to regulate the levels of Zn(2+) in the cytoplasm and organellar compartments to maintain homeostasis. We present a protocol to measure changes in cellular zinc concentrations using either a low-affinity membrane permeable or a high-affinity membrane impermeable fluorescent dye. Overall, zinc-specific fluorescent indicators using the assay can reliably detect the Zn(2+) flux into or out of cultured cells. For complete details on the use and execution of this protocol, please refer to Sanchez et al. (2019).
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spelling pubmed-75802192020-10-26 Protocol for Quantifying Zinc Flux in Cultured Cells using Fluorescent Indicators Ali, Saima Cuajungco, Math P. STAR Protoc Protocol Zinc (Zn(2+)) plays a vital role in the functioning of the cell. Cells have influx and efflux zinc transporters to regulate the levels of Zn(2+) in the cytoplasm and organellar compartments to maintain homeostasis. We present a protocol to measure changes in cellular zinc concentrations using either a low-affinity membrane permeable or a high-affinity membrane impermeable fluorescent dye. Overall, zinc-specific fluorescent indicators using the assay can reliably detect the Zn(2+) flux into or out of cultured cells. For complete details on the use and execution of this protocol, please refer to Sanchez et al. (2019). Elsevier 2020-06-08 /pmc/articles/PMC7580219/ /pubmed/33111096 http://dx.doi.org/10.1016/j.xpro.2020.100050 Text en © 2020 The Author(s) http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Protocol
Ali, Saima
Cuajungco, Math P.
Protocol for Quantifying Zinc Flux in Cultured Cells using Fluorescent Indicators
title Protocol for Quantifying Zinc Flux in Cultured Cells using Fluorescent Indicators
title_full Protocol for Quantifying Zinc Flux in Cultured Cells using Fluorescent Indicators
title_fullStr Protocol for Quantifying Zinc Flux in Cultured Cells using Fluorescent Indicators
title_full_unstemmed Protocol for Quantifying Zinc Flux in Cultured Cells using Fluorescent Indicators
title_short Protocol for Quantifying Zinc Flux in Cultured Cells using Fluorescent Indicators
title_sort protocol for quantifying zinc flux in cultured cells using fluorescent indicators
topic Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7580219/
https://www.ncbi.nlm.nih.gov/pubmed/33111096
http://dx.doi.org/10.1016/j.xpro.2020.100050
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