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Multiplexed and Reiterative Fluorescence Labeling via DNA Circuitry
A class of reactive DNA circuits was adapted as erasable molecular imaging probes that allow fluorescent reporting complexes to be assembled and disassembled on a biological specimen. Circuit reactions are sequence-dependent and therefore facilitate multiplexed (multicolor) detection. Yet, the abili...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2010
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002180/ https://www.ncbi.nlm.nih.gov/pubmed/21080622 http://dx.doi.org/10.1021/bc100348q |
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author | Duose, Dzifa Y. Schweller, Ryan M. Hittelman, Walter N. Diehl, Michael R. |
author_facet | Duose, Dzifa Y. Schweller, Ryan M. Hittelman, Walter N. Diehl, Michael R. |
author_sort | Duose, Dzifa Y. |
collection | PubMed |
description | A class of reactive DNA circuits was adapted as erasable molecular imaging probes that allow fluorescent reporting complexes to be assembled and disassembled on a biological specimen. Circuit reactions are sequence-dependent and therefore facilitate multiplexed (multicolor) detection. Yet, the ability to disassemble reporting complexes also allows fluorophores to be removed and new circuit complexes to be used to label additional markers. Thus, these probes present opportunities to increase the total number of molecular targets that can be visualized on a biological sample by allowing multiple rounds of fluorescence microscopy to be performed. |
format | Text |
id | pubmed-3002180 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-30021802010-12-15 Multiplexed and Reiterative Fluorescence Labeling via DNA Circuitry Duose, Dzifa Y. Schweller, Ryan M. Hittelman, Walter N. Diehl, Michael R. Bioconjug Chem A class of reactive DNA circuits was adapted as erasable molecular imaging probes that allow fluorescent reporting complexes to be assembled and disassembled on a biological specimen. Circuit reactions are sequence-dependent and therefore facilitate multiplexed (multicolor) detection. Yet, the ability to disassemble reporting complexes also allows fluorophores to be removed and new circuit complexes to be used to label additional markers. Thus, these probes present opportunities to increase the total number of molecular targets that can be visualized on a biological sample by allowing multiple rounds of fluorescence microscopy to be performed. American Chemical Society 2010-11-16 2010-12-15 /pmc/articles/PMC3002180/ /pubmed/21080622 http://dx.doi.org/10.1021/bc100348q Text en Copyright © 2010 American Chemical Society http://pubs.acs.org This is an open-access article distributed under the ACS AuthorChoice Terms & Conditions. Any use of this article, must conform to the terms of that license which are available at http://pubs.acs.org. |
spellingShingle | Duose, Dzifa Y. Schweller, Ryan M. Hittelman, Walter N. Diehl, Michael R. Multiplexed and Reiterative Fluorescence Labeling via DNA Circuitry |
title | Multiplexed and Reiterative Fluorescence Labeling via DNA Circuitry |
title_full | Multiplexed and Reiterative Fluorescence Labeling via DNA Circuitry |
title_fullStr | Multiplexed and Reiterative Fluorescence Labeling via DNA Circuitry |
title_full_unstemmed | Multiplexed and Reiterative Fluorescence Labeling via DNA Circuitry |
title_short | Multiplexed and Reiterative Fluorescence Labeling via DNA Circuitry |
title_sort | multiplexed and reiterative fluorescence labeling via dna circuitry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002180/ https://www.ncbi.nlm.nih.gov/pubmed/21080622 http://dx.doi.org/10.1021/bc100348q |
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