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RNA Signal Amplifier Circuit with Integrated Fluorescence Output

[Image: see text] We designed an in vitro signal amplification circuit that takes a short RNA input that catalytically activates the Spinach RNA aptamer to produce a fluorescent output. The circuit consists of three RNA strands: an internally blocked Spinach aptamer, a fuel strand, and an input stra...

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Detalles Bibliográficos
Autores principales: Akter, Farhima, Yokobayashi, Yohei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2014
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487219/
https://www.ncbi.nlm.nih.gov/pubmed/25354355
http://dx.doi.org/10.1021/sb500314r
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author Akter, Farhima
Yokobayashi, Yohei
author_facet Akter, Farhima
Yokobayashi, Yohei
author_sort Akter, Farhima
collection PubMed
description [Image: see text] We designed an in vitro signal amplification circuit that takes a short RNA input that catalytically activates the Spinach RNA aptamer to produce a fluorescent output. The circuit consists of three RNA strands: an internally blocked Spinach aptamer, a fuel strand, and an input strand (catalyst), as well as the Spinach aptamer ligand 3,5-difluoro-4-hydroxylbenzylidene imidazolinone (DFHBI). The input strand initially displaces the internal inhibitory strand to activate the fluorescent aptamer while exposing a toehold to which the fuel strand can bind to further displace and recycle the input strand. Under a favorable condition, one input strand was able to activate up to five molecules of the internally blocked Spinach aptamer in 185 min at 30 °C. The simple RNA circuit reported here serves as a model for catalytic activation of arbitrary RNA effectors by chemical triggers.
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spelling pubmed-44872192015-10-29 RNA Signal Amplifier Circuit with Integrated Fluorescence Output Akter, Farhima Yokobayashi, Yohei ACS Synth Biol [Image: see text] We designed an in vitro signal amplification circuit that takes a short RNA input that catalytically activates the Spinach RNA aptamer to produce a fluorescent output. The circuit consists of three RNA strands: an internally blocked Spinach aptamer, a fuel strand, and an input strand (catalyst), as well as the Spinach aptamer ligand 3,5-difluoro-4-hydroxylbenzylidene imidazolinone (DFHBI). The input strand initially displaces the internal inhibitory strand to activate the fluorescent aptamer while exposing a toehold to which the fuel strand can bind to further displace and recycle the input strand. Under a favorable condition, one input strand was able to activate up to five molecules of the internally blocked Spinach aptamer in 185 min at 30 °C. The simple RNA circuit reported here serves as a model for catalytic activation of arbitrary RNA effectors by chemical triggers. American Chemical Society 2014-10-29 2015-05-15 /pmc/articles/PMC4487219/ /pubmed/25354355 http://dx.doi.org/10.1021/sb500314r Text en Copyright © 2014 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes.
spellingShingle Akter, Farhima
Yokobayashi, Yohei
RNA Signal Amplifier Circuit with Integrated Fluorescence Output
title RNA Signal Amplifier Circuit with Integrated Fluorescence Output
title_full RNA Signal Amplifier Circuit with Integrated Fluorescence Output
title_fullStr RNA Signal Amplifier Circuit with Integrated Fluorescence Output
title_full_unstemmed RNA Signal Amplifier Circuit with Integrated Fluorescence Output
title_short RNA Signal Amplifier Circuit with Integrated Fluorescence Output
title_sort rna signal amplifier circuit with integrated fluorescence output
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4487219/
https://www.ncbi.nlm.nih.gov/pubmed/25354355
http://dx.doi.org/10.1021/sb500314r
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