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Real-Time Detection of a Self-Replicating RNA Enzyme

A system was developed to detect the self-replication of an RNA enzyme in real time. The enzyme is an RNA ligase that undergoes exponential amplification at a constant temperature and can be made to operate in a ligand-dependent manner. The real-time system is based on a fluorimetric readout that di...

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Detalles Bibliográficos
Autores principales: Olea, Charles, Joyce, Gerald F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108293/
https://www.ncbi.nlm.nih.gov/pubmed/27706059
http://dx.doi.org/10.3390/molecules21101310
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author Olea, Charles
Joyce, Gerald F.
author_facet Olea, Charles
Joyce, Gerald F.
author_sort Olea, Charles
collection PubMed
description A system was developed to detect the self-replication of an RNA enzyme in real time. The enzyme is an RNA ligase that undergoes exponential amplification at a constant temperature and can be made to operate in a ligand-dependent manner. The real-time system is based on a fluorimetric readout that directly couples the ligation event to an increase in florescence signal that can be monitored using standard instrumentation. The real-time system can also operate entirely with l-RNA, which is not susceptible to degradation by ribonucleases that are present in biological samples. The system is analogous to real-time PCR, but with the potential to detect small molecules, proteins, and other targets that can be recognized by a suitable aptamer. The ligand-dependent self-replication of RNA has potential applications in molecular diagnostics and biosensing that benefit from the rapid, precise, and real-time detection of various target molecules.
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spelling pubmed-51082932017-09-30 Real-Time Detection of a Self-Replicating RNA Enzyme Olea, Charles Joyce, Gerald F. Molecules Article A system was developed to detect the self-replication of an RNA enzyme in real time. The enzyme is an RNA ligase that undergoes exponential amplification at a constant temperature and can be made to operate in a ligand-dependent manner. The real-time system is based on a fluorimetric readout that directly couples the ligation event to an increase in florescence signal that can be monitored using standard instrumentation. The real-time system can also operate entirely with l-RNA, which is not susceptible to degradation by ribonucleases that are present in biological samples. The system is analogous to real-time PCR, but with the potential to detect small molecules, proteins, and other targets that can be recognized by a suitable aptamer. The ligand-dependent self-replication of RNA has potential applications in molecular diagnostics and biosensing that benefit from the rapid, precise, and real-time detection of various target molecules. MDPI 2016-09-30 /pmc/articles/PMC5108293/ /pubmed/27706059 http://dx.doi.org/10.3390/molecules21101310 Text en © 2016 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC-BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Olea, Charles
Joyce, Gerald F.
Real-Time Detection of a Self-Replicating RNA Enzyme
title Real-Time Detection of a Self-Replicating RNA Enzyme
title_full Real-Time Detection of a Self-Replicating RNA Enzyme
title_fullStr Real-Time Detection of a Self-Replicating RNA Enzyme
title_full_unstemmed Real-Time Detection of a Self-Replicating RNA Enzyme
title_short Real-Time Detection of a Self-Replicating RNA Enzyme
title_sort real-time detection of a self-replicating rna enzyme
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5108293/
https://www.ncbi.nlm.nih.gov/pubmed/27706059
http://dx.doi.org/10.3390/molecules21101310
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