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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...

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Autores principales: Duose, Dzifa Y., Schweller, Ryan M., Hittelman, Walter N., Diehl, Michael R.
Formato: Texto
Lenguaje:English
Publicado: American Chemical Society 2010
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.
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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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