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Incorporation of quantum dots on virus in polycationic solution
Developing methods to label viruses with fluorescent moieties has its merits in elucidating viral infection mechanisms and exploring novel antiviral therapeutics. Fluorescent quantum dots (QDs), an emerging probe for biological imaging and medical diagnostics, were employed in this study to tag retr...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
Dove Medical Press
2006
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426762/ https://www.ncbi.nlm.nih.gov/pubmed/17722262 |
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author | You, Jin-Oh Liu, Yu-San Liu, Yu-Chuan Joo, Kye-II Peng, Ching-An |
author_facet | You, Jin-Oh Liu, Yu-San Liu, Yu-Chuan Joo, Kye-II Peng, Ching-An |
author_sort | You, Jin-Oh |
collection | PubMed |
description | Developing methods to label viruses with fluorescent moieties has its merits in elucidating viral infection mechanisms and exploring novel antiviral therapeutics. Fluorescent quantum dots (QDs), an emerging probe for biological imaging and medical diagnostics, were employed in this study to tag retrovirus encoding enhanced green fluorescent protein (EGFP) genes. Electrostatic repulsion forces generated from both negatively charged retrovirus and QDs were neutralized by cationic Polybrene(®), forming colloidal complexes of QDs–virus. By examining the level of EGFP expression in 3T3 fibroblast cells treated with QDs-tagged retroviruses for 24 hours, the infectivity of retrovirus incorporated with QDs was shown to be only slightly decreased. Moreover, the imaging of QDs can be detected in the cellular milieu. In summary, the mild method developed here makes QDs-tagged virus a potential imaging probe for direct tracking the infection process and monitoring distribution of viral particles in infected cells. |
format | Text |
id | pubmed-2426762 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2006 |
publisher | Dove Medical Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-24267622008-06-20 Incorporation of quantum dots on virus in polycationic solution You, Jin-Oh Liu, Yu-San Liu, Yu-Chuan Joo, Kye-II Peng, Ching-An Int J Nanomedicine Original Research Developing methods to label viruses with fluorescent moieties has its merits in elucidating viral infection mechanisms and exploring novel antiviral therapeutics. Fluorescent quantum dots (QDs), an emerging probe for biological imaging and medical diagnostics, were employed in this study to tag retrovirus encoding enhanced green fluorescent protein (EGFP) genes. Electrostatic repulsion forces generated from both negatively charged retrovirus and QDs were neutralized by cationic Polybrene(®), forming colloidal complexes of QDs–virus. By examining the level of EGFP expression in 3T3 fibroblast cells treated with QDs-tagged retroviruses for 24 hours, the infectivity of retrovirus incorporated with QDs was shown to be only slightly decreased. Moreover, the imaging of QDs can be detected in the cellular milieu. In summary, the mild method developed here makes QDs-tagged virus a potential imaging probe for direct tracking the infection process and monitoring distribution of viral particles in infected cells. Dove Medical Press 2006-03 /pmc/articles/PMC2426762/ /pubmed/17722262 Text en © 2006 Dove Medical Press Limited. All rights reserved |
spellingShingle | Original Research You, Jin-Oh Liu, Yu-San Liu, Yu-Chuan Joo, Kye-II Peng, Ching-An Incorporation of quantum dots on virus in polycationic solution |
title | Incorporation of quantum dots on virus in polycationic solution |
title_full | Incorporation of quantum dots on virus in polycationic solution |
title_fullStr | Incorporation of quantum dots on virus in polycationic solution |
title_full_unstemmed | Incorporation of quantum dots on virus in polycationic solution |
title_short | Incorporation of quantum dots on virus in polycationic solution |
title_sort | incorporation of quantum dots on virus in polycationic solution |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2426762/ https://www.ncbi.nlm.nih.gov/pubmed/17722262 |
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