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FRET-Based Nanobiosensors for Imaging Intracellular Ca(2+) and H(+) Microdomains

Semiconductor nanocrystals (NCs) or quantum dots (QDs) are luminous point emitters increasingly being used to tag and track biomolecules in biological/biomedical imaging. However, their intracellular use as highlighters of single-molecule localization and nanobiosensors reporting ion microdomains ch...

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Autores principales: Zamaleeva, Alsu I., Despras, Guillaume, Luccardini, Camilla, Collot, Mayeul, de Waard, Michel, Oheim, Martin, Mallet, Jean-Maurice, Feltz, Anne
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610457/
https://www.ncbi.nlm.nih.gov/pubmed/26404317
http://dx.doi.org/10.3390/s150924662
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author Zamaleeva, Alsu I.
Despras, Guillaume
Luccardini, Camilla
Collot, Mayeul
de Waard, Michel
Oheim, Martin
Mallet, Jean-Maurice
Feltz, Anne
author_facet Zamaleeva, Alsu I.
Despras, Guillaume
Luccardini, Camilla
Collot, Mayeul
de Waard, Michel
Oheim, Martin
Mallet, Jean-Maurice
Feltz, Anne
author_sort Zamaleeva, Alsu I.
collection PubMed
description Semiconductor nanocrystals (NCs) or quantum dots (QDs) are luminous point emitters increasingly being used to tag and track biomolecules in biological/biomedical imaging. However, their intracellular use as highlighters of single-molecule localization and nanobiosensors reporting ion microdomains changes has remained a major challenge. Here, we report the design, generation and validation of FRET-based nanobiosensors for detection of intracellular Ca(2+) and H(+) transients. Our sensors combine a commercially available CANdot(®)565QD as an energy donor with, as an acceptor, our custom-synthesized red-emitting Ca(2+) or H(+) probes. These ‘Rubies’ are based on an extended rhodamine as a fluorophore and a phenol or BAPTA (1,2-bis(o-aminophenoxy)ethane-N,N,N′,N′-tetra-acetic acid) for H(+) or Ca(2+) sensing, respectively, and additionally bear a linker arm for conjugation. QDs were stably functionalized using the same SH/maleimide crosslink chemistry for all desired reactants. Mixing ion sensor and cell-penetrating peptides (that facilitate cytoplasmic delivery) at the desired stoichiometric ratio produced controlled multi-conjugated assemblies. Multiple acceptors on the same central donor allow up-concentrating the ion sensor on the QD surface to concentrations higher than those that could be achieved in free solution, increasing FRET efficiency and improving the signal. We validate these nanosensors for the detection of intracellular Ca(2+) and pH transients using live-cell fluorescence imaging.
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spelling pubmed-46104572015-10-26 FRET-Based Nanobiosensors for Imaging Intracellular Ca(2+) and H(+) Microdomains Zamaleeva, Alsu I. Despras, Guillaume Luccardini, Camilla Collot, Mayeul de Waard, Michel Oheim, Martin Mallet, Jean-Maurice Feltz, Anne Sensors (Basel) Article Semiconductor nanocrystals (NCs) or quantum dots (QDs) are luminous point emitters increasingly being used to tag and track biomolecules in biological/biomedical imaging. However, their intracellular use as highlighters of single-molecule localization and nanobiosensors reporting ion microdomains changes has remained a major challenge. Here, we report the design, generation and validation of FRET-based nanobiosensors for detection of intracellular Ca(2+) and H(+) transients. Our sensors combine a commercially available CANdot(®)565QD as an energy donor with, as an acceptor, our custom-synthesized red-emitting Ca(2+) or H(+) probes. These ‘Rubies’ are based on an extended rhodamine as a fluorophore and a phenol or BAPTA (1,2-bis(o-aminophenoxy)ethane-N,N,N′,N′-tetra-acetic acid) for H(+) or Ca(2+) sensing, respectively, and additionally bear a linker arm for conjugation. QDs were stably functionalized using the same SH/maleimide crosslink chemistry for all desired reactants. Mixing ion sensor and cell-penetrating peptides (that facilitate cytoplasmic delivery) at the desired stoichiometric ratio produced controlled multi-conjugated assemblies. Multiple acceptors on the same central donor allow up-concentrating the ion sensor on the QD surface to concentrations higher than those that could be achieved in free solution, increasing FRET efficiency and improving the signal. We validate these nanosensors for the detection of intracellular Ca(2+) and pH transients using live-cell fluorescence imaging. MDPI 2015-09-23 /pmc/articles/PMC4610457/ /pubmed/26404317 http://dx.doi.org/10.3390/s150924662 Text en © 2015 by the authors; licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Zamaleeva, Alsu I.
Despras, Guillaume
Luccardini, Camilla
Collot, Mayeul
de Waard, Michel
Oheim, Martin
Mallet, Jean-Maurice
Feltz, Anne
FRET-Based Nanobiosensors for Imaging Intracellular Ca(2+) and H(+) Microdomains
title FRET-Based Nanobiosensors for Imaging Intracellular Ca(2+) and H(+) Microdomains
title_full FRET-Based Nanobiosensors for Imaging Intracellular Ca(2+) and H(+) Microdomains
title_fullStr FRET-Based Nanobiosensors for Imaging Intracellular Ca(2+) and H(+) Microdomains
title_full_unstemmed FRET-Based Nanobiosensors for Imaging Intracellular Ca(2+) and H(+) Microdomains
title_short FRET-Based Nanobiosensors for Imaging Intracellular Ca(2+) and H(+) Microdomains
title_sort fret-based nanobiosensors for imaging intracellular ca(2+) and h(+) microdomains
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4610457/
https://www.ncbi.nlm.nih.gov/pubmed/26404317
http://dx.doi.org/10.3390/s150924662
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