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Design of Biotin-Functionalized Luminescent Quantum Dots

We report the design and synthesis of a tetraethylene glycol- (TEG-) based bidentate ligand functionalized with dihydrolipoic acid (DHLA) and biotin (DHLA—TEG—biotin) to promote biocompatibility of luminescent quantum dots (QD's). This new ligand readily binds to CdSe—ZnS core-shell QDs via sur...

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Detalles Bibliográficos
Autores principales: Susumu, Kimihiro, Uyeda, H. Tetsuo, Medintz, Igor L., Mattoussi, Hedi
Formato: Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276867/
https://www.ncbi.nlm.nih.gov/pubmed/18382625
http://dx.doi.org/10.1155/2007/90651
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author Susumu, Kimihiro
Uyeda, H. Tetsuo
Medintz, Igor L.
Mattoussi, Hedi
author_facet Susumu, Kimihiro
Uyeda, H. Tetsuo
Medintz, Igor L.
Mattoussi, Hedi
author_sort Susumu, Kimihiro
collection PubMed
description We report the design and synthesis of a tetraethylene glycol- (TEG-) based bidentate ligand functionalized with dihydrolipoic acid (DHLA) and biotin (DHLA—TEG—biotin) to promote biocompatibility of luminescent quantum dots (QD's). This new ligand readily binds to CdSe—ZnS core-shell QDs via surface ligand exchange. QDs capped with a mixture of DHLA and DHLA—TEG—biotin or polyethylene glycol- (PEG-) (molecular weight average ∼600) modified DHLA (DHLA—PEG600) and DHLA—TEG—biotin are easily dispersed in aqueous buffer solutions. In particular, homogeneous buffer solutions of QDs capped with a mixture of DHLA—PEG600 and DHLA—TEG—biotin that are stable over broad pH range have been prepared. QDs coated with mixtures of DHLA/DHLA—TEG—biotin and with DHLA—PEG600/DHLA—TEG—biotin were tested in surface binding assays and the results indicate that biotin groups on the QD surface interact specifically with NeutrAvidin-functionalized microtiter well plates.
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spelling pubmed-22768672008-04-01 Design of Biotin-Functionalized Luminescent Quantum Dots Susumu, Kimihiro Uyeda, H. Tetsuo Medintz, Igor L. Mattoussi, Hedi J Biomed Biotechnol Research Article We report the design and synthesis of a tetraethylene glycol- (TEG-) based bidentate ligand functionalized with dihydrolipoic acid (DHLA) and biotin (DHLA—TEG—biotin) to promote biocompatibility of luminescent quantum dots (QD's). This new ligand readily binds to CdSe—ZnS core-shell QDs via surface ligand exchange. QDs capped with a mixture of DHLA and DHLA—TEG—biotin or polyethylene glycol- (PEG-) (molecular weight average ∼600) modified DHLA (DHLA—PEG600) and DHLA—TEG—biotin are easily dispersed in aqueous buffer solutions. In particular, homogeneous buffer solutions of QDs capped with a mixture of DHLA—PEG600 and DHLA—TEG—biotin that are stable over broad pH range have been prepared. QDs coated with mixtures of DHLA/DHLA—TEG—biotin and with DHLA—PEG600/DHLA—TEG—biotin were tested in surface binding assays and the results indicate that biotin groups on the QD surface interact specifically with NeutrAvidin-functionalized microtiter well plates. Hindawi Publishing Corporation 2007 2008-03-18 /pmc/articles/PMC2276867/ /pubmed/18382625 http://dx.doi.org/10.1155/2007/90651 Text en Copyright © 2007 Kimihiro Susumu et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Susumu, Kimihiro
Uyeda, H. Tetsuo
Medintz, Igor L.
Mattoussi, Hedi
Design of Biotin-Functionalized Luminescent Quantum Dots
title Design of Biotin-Functionalized Luminescent Quantum Dots
title_full Design of Biotin-Functionalized Luminescent Quantum Dots
title_fullStr Design of Biotin-Functionalized Luminescent Quantum Dots
title_full_unstemmed Design of Biotin-Functionalized Luminescent Quantum Dots
title_short Design of Biotin-Functionalized Luminescent Quantum Dots
title_sort design of biotin-functionalized luminescent quantum dots
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2276867/
https://www.ncbi.nlm.nih.gov/pubmed/18382625
http://dx.doi.org/10.1155/2007/90651
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