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Fluorescence-tagged metallothionein with CdTe quantum dots analyzed by the chip-CE technique

ABSTRACT: Quantum dots (QDs) are fluorescence nanoparticles (NPs) with unique optic properties which allow their use as probes in chemical, biological, immunological, and molecular imaging. QDs linked with target ligands such as peptides or small molecules can be used as tumor biomarkers. These part...

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Autores principales: Guszpit, Ewelina, Krizkova, Sona, Kepinska, Marta, Rodrigo, Miguel Angel Merlos, Milnerowicz, Halina, Kopel, Pavel, Kizek, Rene
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624813/
https://www.ncbi.nlm.nih.gov/pubmed/26543399
http://dx.doi.org/10.1007/s11051-015-3226-8
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author Guszpit, Ewelina
Krizkova, Sona
Kepinska, Marta
Rodrigo, Miguel Angel Merlos
Milnerowicz, Halina
Kopel, Pavel
Kizek, Rene
author_facet Guszpit, Ewelina
Krizkova, Sona
Kepinska, Marta
Rodrigo, Miguel Angel Merlos
Milnerowicz, Halina
Kopel, Pavel
Kizek, Rene
author_sort Guszpit, Ewelina
collection PubMed
description ABSTRACT: Quantum dots (QDs) are fluorescence nanoparticles (NPs) with unique optic properties which allow their use as probes in chemical, biological, immunological, and molecular imaging. QDs linked with target ligands such as peptides or small molecules can be used as tumor biomarkers. These particles are a promising tool for selective, fast, and sensitive tagging and imaging in medicine. In this study, an attempt was made to use QDs as a marker for human metallothionein (MT) isoforms 1 and 2. Four kinds of CdTe QDs of different sizes bioconjugated with MT were analyzed using the chip-CE technique. Based on the results, it can be concluded that MT is willing to interact with QDs, and the chip-CE technique enables the observation of their complexes. It was also observed that changes ranging roughly 6–7 kDa, a value corresponding to the MT monomer, depend on the hydrodynamic diameters of QDs; also, the MT sample without cadmium interacted stronger with QDs than MT saturated with cadmium. Results show that MT is willing to interact with smaller QDs (blue CdTe) rather than larger ones QDs (red CdTe). To our knowledge, chip-CE has not previously been applied in the study of CdTe QDs interaction with MT. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11051-015-3226-8) contains supplementary material, which is available to authorized users.
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spelling pubmed-46248132015-11-03 Fluorescence-tagged metallothionein with CdTe quantum dots analyzed by the chip-CE technique Guszpit, Ewelina Krizkova, Sona Kepinska, Marta Rodrigo, Miguel Angel Merlos Milnerowicz, Halina Kopel, Pavel Kizek, Rene J Nanopart Res Research Paper ABSTRACT: Quantum dots (QDs) are fluorescence nanoparticles (NPs) with unique optic properties which allow their use as probes in chemical, biological, immunological, and molecular imaging. QDs linked with target ligands such as peptides or small molecules can be used as tumor biomarkers. These particles are a promising tool for selective, fast, and sensitive tagging and imaging in medicine. In this study, an attempt was made to use QDs as a marker for human metallothionein (MT) isoforms 1 and 2. Four kinds of CdTe QDs of different sizes bioconjugated with MT were analyzed using the chip-CE technique. Based on the results, it can be concluded that MT is willing to interact with QDs, and the chip-CE technique enables the observation of their complexes. It was also observed that changes ranging roughly 6–7 kDa, a value corresponding to the MT monomer, depend on the hydrodynamic diameters of QDs; also, the MT sample without cadmium interacted stronger with QDs than MT saturated with cadmium. Results show that MT is willing to interact with smaller QDs (blue CdTe) rather than larger ones QDs (red CdTe). To our knowledge, chip-CE has not previously been applied in the study of CdTe QDs interaction with MT. GRAPHICAL ABSTRACT: [Image: see text] ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s11051-015-3226-8) contains supplementary material, which is available to authorized users. Springer Netherlands 2015-10-28 2015 /pmc/articles/PMC4624813/ /pubmed/26543399 http://dx.doi.org/10.1007/s11051-015-3226-8 Text en © The Author(s) 2015 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Research Paper
Guszpit, Ewelina
Krizkova, Sona
Kepinska, Marta
Rodrigo, Miguel Angel Merlos
Milnerowicz, Halina
Kopel, Pavel
Kizek, Rene
Fluorescence-tagged metallothionein with CdTe quantum dots analyzed by the chip-CE technique
title Fluorescence-tagged metallothionein with CdTe quantum dots analyzed by the chip-CE technique
title_full Fluorescence-tagged metallothionein with CdTe quantum dots analyzed by the chip-CE technique
title_fullStr Fluorescence-tagged metallothionein with CdTe quantum dots analyzed by the chip-CE technique
title_full_unstemmed Fluorescence-tagged metallothionein with CdTe quantum dots analyzed by the chip-CE technique
title_short Fluorescence-tagged metallothionein with CdTe quantum dots analyzed by the chip-CE technique
title_sort fluorescence-tagged metallothionein with cdte quantum dots analyzed by the chip-ce technique
topic Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4624813/
https://www.ncbi.nlm.nih.gov/pubmed/26543399
http://dx.doi.org/10.1007/s11051-015-3226-8
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