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CdSe Quantum Dots in Human Models Derived from ALS Patients: Characterization, Nuclear Penetration Studies and Multiplexing
CdSe quantum dots (QDs) are valuable tools for deciphering molecular mechanisms in cells. Their conjugation with antibodies offers a unique staining source with optimal characteristics, including increased photostability and narrow emission spectra, allowing for improved multiplexing capabilities us...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998605/ https://www.ncbi.nlm.nih.gov/pubmed/33803158 http://dx.doi.org/10.3390/nano11030671 |
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author | Tosat-Bitrián, Carlota Avis-Bodas, Alicia Porras, Gracia Borrego-Hernández, Daniel García-Redondo, Alberto Martín-Requero, Angeles Palomo, Valle |
author_facet | Tosat-Bitrián, Carlota Avis-Bodas, Alicia Porras, Gracia Borrego-Hernández, Daniel García-Redondo, Alberto Martín-Requero, Angeles Palomo, Valle |
author_sort | Tosat-Bitrián, Carlota |
collection | PubMed |
description | CdSe quantum dots (QDs) are valuable tools for deciphering molecular mechanisms in cells. Their conjugation with antibodies offers a unique staining source with optimal characteristics, including increased photostability and narrow emission spectra, allowing for improved multiplexing capabilities using a single excitation source. In combination with pathology models derived from patients, they have great potential to contribute to quantitative molecular profiling and promote personalized medicine. However, the commercial availability of diverse CdSe QDs is still limited and characterization techniques must be performed to these materials or the conjugates developed in the lab to assure a proper function and reproducibility. Furthermore, while there is significant data of QDs experiments in cell lines, the literature with primary human cells is scarce, and QD behavior in these systems may be different. Rigorous characterization data of commercially available QDs and their conjugates with biomolecules of interest is needed in order to establish their potential for target labelling and expand their use among research labs. Here we compare the characterization and labelling performance of different QD conjugates in SH-SY5Y cell line, fibroblasts and immortalized lymphocytes derived from amyotrophic lateral sclerosis patients. |
format | Online Article Text |
id | pubmed-7998605 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-79986052021-03-28 CdSe Quantum Dots in Human Models Derived from ALS Patients: Characterization, Nuclear Penetration Studies and Multiplexing Tosat-Bitrián, Carlota Avis-Bodas, Alicia Porras, Gracia Borrego-Hernández, Daniel García-Redondo, Alberto Martín-Requero, Angeles Palomo, Valle Nanomaterials (Basel) Article CdSe quantum dots (QDs) are valuable tools for deciphering molecular mechanisms in cells. Their conjugation with antibodies offers a unique staining source with optimal characteristics, including increased photostability and narrow emission spectra, allowing for improved multiplexing capabilities using a single excitation source. In combination with pathology models derived from patients, they have great potential to contribute to quantitative molecular profiling and promote personalized medicine. However, the commercial availability of diverse CdSe QDs is still limited and characterization techniques must be performed to these materials or the conjugates developed in the lab to assure a proper function and reproducibility. Furthermore, while there is significant data of QDs experiments in cell lines, the literature with primary human cells is scarce, and QD behavior in these systems may be different. Rigorous characterization data of commercially available QDs and their conjugates with biomolecules of interest is needed in order to establish their potential for target labelling and expand their use among research labs. Here we compare the characterization and labelling performance of different QD conjugates in SH-SY5Y cell line, fibroblasts and immortalized lymphocytes derived from amyotrophic lateral sclerosis patients. MDPI 2021-03-09 /pmc/articles/PMC7998605/ /pubmed/33803158 http://dx.doi.org/10.3390/nano11030671 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ). |
spellingShingle | Article Tosat-Bitrián, Carlota Avis-Bodas, Alicia Porras, Gracia Borrego-Hernández, Daniel García-Redondo, Alberto Martín-Requero, Angeles Palomo, Valle CdSe Quantum Dots in Human Models Derived from ALS Patients: Characterization, Nuclear Penetration Studies and Multiplexing |
title | CdSe Quantum Dots in Human Models Derived from ALS Patients: Characterization, Nuclear Penetration Studies and Multiplexing |
title_full | CdSe Quantum Dots in Human Models Derived from ALS Patients: Characterization, Nuclear Penetration Studies and Multiplexing |
title_fullStr | CdSe Quantum Dots in Human Models Derived from ALS Patients: Characterization, Nuclear Penetration Studies and Multiplexing |
title_full_unstemmed | CdSe Quantum Dots in Human Models Derived from ALS Patients: Characterization, Nuclear Penetration Studies and Multiplexing |
title_short | CdSe Quantum Dots in Human Models Derived from ALS Patients: Characterization, Nuclear Penetration Studies and Multiplexing |
title_sort | cdse quantum dots in human models derived from als patients: characterization, nuclear penetration studies and multiplexing |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7998605/ https://www.ncbi.nlm.nih.gov/pubmed/33803158 http://dx.doi.org/10.3390/nano11030671 |
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