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DNA-Based Assembly of Quantum Dots into Dimers and Helices

Owing to their unique optical properties, colloidal quantum dots (QDs) have attracted much attention as versatile fluorescent markers with broad biological and physical applications. On the other hand, DNA-based assembly has proven to be a powerful bottom-up approach to create designer nanoscale obj...

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Detalles Bibliográficos
Autores principales: Zhang, Tao, Liedl, Tim
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473979/
https://www.ncbi.nlm.nih.gov/pubmed/30832359
http://dx.doi.org/10.3390/nano9030339
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author Zhang, Tao
Liedl, Tim
author_facet Zhang, Tao
Liedl, Tim
author_sort Zhang, Tao
collection PubMed
description Owing to their unique optical properties, colloidal quantum dots (QDs) have attracted much attention as versatile fluorescent markers with broad biological and physical applications. On the other hand, DNA-based assembly has proven to be a powerful bottom-up approach to create designer nanoscale objects and to use these objects for the site-directed arrangement of guest components. To achieve good colloidal stability and accurate positioning of QDs on DNA templates, robust QD surface functionalization is crucial. Here, we present a simple and reliable conjugation method for the direct attachment of DNA molecules to QDs. Phosphorothiolated regions of chimera oligonucleotides are attached and incorporated into a ZnS layer freshly growing in situ on QDs that were rendered water soluble with hydrophilic ligands in a prior step. The reaction can be completed in a 2 mL plastic tube without any special equipment. The utility of these DNA-labeled QDs is demonstrated via prototypical assemblies such as QDs dimers with various spacings and chiral helical architectures.
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spelling pubmed-64739792019-05-03 DNA-Based Assembly of Quantum Dots into Dimers and Helices Zhang, Tao Liedl, Tim Nanomaterials (Basel) Communication Owing to their unique optical properties, colloidal quantum dots (QDs) have attracted much attention as versatile fluorescent markers with broad biological and physical applications. On the other hand, DNA-based assembly has proven to be a powerful bottom-up approach to create designer nanoscale objects and to use these objects for the site-directed arrangement of guest components. To achieve good colloidal stability and accurate positioning of QDs on DNA templates, robust QD surface functionalization is crucial. Here, we present a simple and reliable conjugation method for the direct attachment of DNA molecules to QDs. Phosphorothiolated regions of chimera oligonucleotides are attached and incorporated into a ZnS layer freshly growing in situ on QDs that were rendered water soluble with hydrophilic ligands in a prior step. The reaction can be completed in a 2 mL plastic tube without any special equipment. The utility of these DNA-labeled QDs is demonstrated via prototypical assemblies such as QDs dimers with various spacings and chiral helical architectures. MDPI 2019-03-02 /pmc/articles/PMC6473979/ /pubmed/30832359 http://dx.doi.org/10.3390/nano9030339 Text en © 2019 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 (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Communication
Zhang, Tao
Liedl, Tim
DNA-Based Assembly of Quantum Dots into Dimers and Helices
title DNA-Based Assembly of Quantum Dots into Dimers and Helices
title_full DNA-Based Assembly of Quantum Dots into Dimers and Helices
title_fullStr DNA-Based Assembly of Quantum Dots into Dimers and Helices
title_full_unstemmed DNA-Based Assembly of Quantum Dots into Dimers and Helices
title_short DNA-Based Assembly of Quantum Dots into Dimers and Helices
title_sort dna-based assembly of quantum dots into dimers and helices
topic Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6473979/
https://www.ncbi.nlm.nih.gov/pubmed/30832359
http://dx.doi.org/10.3390/nano9030339
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