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A method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging

Optical nanoparticle (NP)-based sensors have been widely implemented as tools for detection of targeted ions and biomolecules. The NP sensing platform offer a modular design that can incorporate different sensing components for greater target specificity and the ability to tune the dynamic range, as...

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Autores principales: Rong, Guoxin, Kim, Eric H., Poskanzer, Kira E., Clark, Heather A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589868/
https://www.ncbi.nlm.nih.gov/pubmed/28883429
http://dx.doi.org/10.1038/s41598-017-11162-8
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author Rong, Guoxin
Kim, Eric H.
Poskanzer, Kira E.
Clark, Heather A.
author_facet Rong, Guoxin
Kim, Eric H.
Poskanzer, Kira E.
Clark, Heather A.
author_sort Rong, Guoxin
collection PubMed
description Optical nanoparticle (NP)-based sensors have been widely implemented as tools for detection of targeted ions and biomolecules. The NP sensing platform offer a modular design that can incorporate different sensing components for greater target specificity and the ability to tune the dynamic range, as well as encapsulation of multiple dyes to generate a ratiometric signal with varying spectra. Despite these advantages, demonstrating quantitative ion imaging for intracellular measurement still possess a major challenge. Here, we describe fundamentals that enable intracellular validation of this approach using ion-selective nanosensors for investigating calcium (Ca(2+)) as a model ion. While conventional indicators can improve individual aspects of indicator performance such as Kd, wavelength, and ratiometric measurements, the use of NP sensors can achieve combined benefits of addressing these issues simultaneously. The nanosensor incorporates highly calcium-selective ionophores and two fluorescence indicators that act as signal transducers to facilitate quantitative ratiometric imaging. For intracellular Ca(2+) application, the sensors are fine-tuned to physiological sensing range, and live-cell imaging and quantification are demonstrated in HeLa cells loaded with nanosensors and their responsiveness to carbachol-evoked store release (~400 nM). The current nanosensor design thus provides a promising sensing platform for real-time detection and optical determination of intracellular ions.
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spelling pubmed-55898682017-09-13 A method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging Rong, Guoxin Kim, Eric H. Poskanzer, Kira E. Clark, Heather A. Sci Rep Article Optical nanoparticle (NP)-based sensors have been widely implemented as tools for detection of targeted ions and biomolecules. The NP sensing platform offer a modular design that can incorporate different sensing components for greater target specificity and the ability to tune the dynamic range, as well as encapsulation of multiple dyes to generate a ratiometric signal with varying spectra. Despite these advantages, demonstrating quantitative ion imaging for intracellular measurement still possess a major challenge. Here, we describe fundamentals that enable intracellular validation of this approach using ion-selective nanosensors for investigating calcium (Ca(2+)) as a model ion. While conventional indicators can improve individual aspects of indicator performance such as Kd, wavelength, and ratiometric measurements, the use of NP sensors can achieve combined benefits of addressing these issues simultaneously. The nanosensor incorporates highly calcium-selective ionophores and two fluorescence indicators that act as signal transducers to facilitate quantitative ratiometric imaging. For intracellular Ca(2+) application, the sensors are fine-tuned to physiological sensing range, and live-cell imaging and quantification are demonstrated in HeLa cells loaded with nanosensors and their responsiveness to carbachol-evoked store release (~400 nM). The current nanosensor design thus provides a promising sensing platform for real-time detection and optical determination of intracellular ions. Nature Publishing Group UK 2017-09-07 /pmc/articles/PMC5589868/ /pubmed/28883429 http://dx.doi.org/10.1038/s41598-017-11162-8 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Rong, Guoxin
Kim, Eric H.
Poskanzer, Kira E.
Clark, Heather A.
A method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging
title A method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging
title_full A method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging
title_fullStr A method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging
title_full_unstemmed A method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging
title_short A method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging
title_sort method for estimating intracellular ion concentration using optical nanosensors and ratiometric imaging
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5589868/
https://www.ncbi.nlm.nih.gov/pubmed/28883429
http://dx.doi.org/10.1038/s41598-017-11162-8
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