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A new G-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition

EcoRI is an important biomacromolecule in live cells and protects bacterial cells against foreign DNA. In this work, we developed a simple and convenient G-triplex (G3) (5′-TGGGAAGGGAGGGAATTCCCT-3′)-based colorimetric assay for the rapid and selective detection of EcoRI activity and inhibition. The...

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Detalles Bibliográficos
Autores principales: Gao, Congcong, Che, Baoquan, Dai, Hong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society of Chemistry 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037997/
https://www.ncbi.nlm.nih.gov/pubmed/35480740
http://dx.doi.org/10.1039/d1ra04203c
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author Gao, Congcong
Che, Baoquan
Dai, Hong
author_facet Gao, Congcong
Che, Baoquan
Dai, Hong
author_sort Gao, Congcong
collection PubMed
description EcoRI is an important biomacromolecule in live cells and protects bacterial cells against foreign DNA. In this work, we developed a simple and convenient G-triplex (G3) (5′-TGGGAAGGGAGGGAATTCCCT-3′)-based colorimetric assay for the rapid and selective detection of EcoRI activity and inhibition. The sequence specifically responds to EcoRI in the presence of K(+) and hemin to form a G-triplex/hemin complex. Taking advantage of G-triplex, EcoRI activity was investigated under the optimized conditions. The absorption intensity ratio displayed a linear relationship against the concentration of EcoRI in the range 0 to 100 U mL(−1), and the detection limit was 5.7 U mL(−1). Furthermore, G3 showed good selectivity, and the ability to be used to screen for EcoRI inhibitors, indicating its potential in detection and analysis applications.
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spelling pubmed-90379972022-04-26 A new G-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition Gao, Congcong Che, Baoquan Dai, Hong RSC Adv Chemistry EcoRI is an important biomacromolecule in live cells and protects bacterial cells against foreign DNA. In this work, we developed a simple and convenient G-triplex (G3) (5′-TGGGAAGGGAGGGAATTCCCT-3′)-based colorimetric assay for the rapid and selective detection of EcoRI activity and inhibition. The sequence specifically responds to EcoRI in the presence of K(+) and hemin to form a G-triplex/hemin complex. Taking advantage of G-triplex, EcoRI activity was investigated under the optimized conditions. The absorption intensity ratio displayed a linear relationship against the concentration of EcoRI in the range 0 to 100 U mL(−1), and the detection limit was 5.7 U mL(−1). Furthermore, G3 showed good selectivity, and the ability to be used to screen for EcoRI inhibitors, indicating its potential in detection and analysis applications. The Royal Society of Chemistry 2021-08-19 /pmc/articles/PMC9037997/ /pubmed/35480740 http://dx.doi.org/10.1039/d1ra04203c Text en This journal is © The Royal Society of Chemistry https://creativecommons.org/licenses/by-nc/3.0/
spellingShingle Chemistry
Gao, Congcong
Che, Baoquan
Dai, Hong
A new G-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition
title A new G-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition
title_full A new G-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition
title_fullStr A new G-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition
title_full_unstemmed A new G-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition
title_short A new G-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition
title_sort new g-triplex-based strategy for sensitivity enhancement of the detection of endonuclease activity and inhibition
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9037997/
https://www.ncbi.nlm.nih.gov/pubmed/35480740
http://dx.doi.org/10.1039/d1ra04203c
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