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Aptameric enzyme subunit for homogeneous DNA sensing

We have developed an aptameric enzyme subunit (AES) which can detect the DNA in a homogeneous solution. The AES is an artificial enzyme subunit composed of an enzyme-inhibiting aptamer bearing a target-molecule binding site. We connected a probe DNA to a thrombin-inhibiting aptamer at its 5′ or 3′ e...

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Detalles Bibliográficos
Autores principales: Ikebukuro, Kazunori, Yoshida, Wataru, Sode, Koji
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Netherlands 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087721/
https://www.ncbi.nlm.nih.gov/pubmed/17849085
http://dx.doi.org/10.1007/s10529-007-9526-z
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author Ikebukuro, Kazunori
Yoshida, Wataru
Sode, Koji
author_facet Ikebukuro, Kazunori
Yoshida, Wataru
Sode, Koji
author_sort Ikebukuro, Kazunori
collection PubMed
description We have developed an aptameric enzyme subunit (AES) which can detect the DNA in a homogeneous solution. The AES is an artificial enzyme subunit composed of an enzyme-inhibiting aptamer bearing a target-molecule binding site. We connected a probe DNA to a thrombin-inhibiting aptamer at its 5′ or 3′ end. The inhibitory activity of the thrombin-inhibiting aptamer bearing the probe DNA decreased compared to that of the original aptamer; however, it recovered upon hybridization with the target DNA. Using this AES, we were able to detect target DNAs by measuring the thrombin activity in a homogeneous solution.
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spelling pubmed-70877212020-03-23 Aptameric enzyme subunit for homogeneous DNA sensing Ikebukuro, Kazunori Yoshida, Wataru Sode, Koji Biotechnol Lett Original Research Paper We have developed an aptameric enzyme subunit (AES) which can detect the DNA in a homogeneous solution. The AES is an artificial enzyme subunit composed of an enzyme-inhibiting aptamer bearing a target-molecule binding site. We connected a probe DNA to a thrombin-inhibiting aptamer at its 5′ or 3′ end. The inhibitory activity of the thrombin-inhibiting aptamer bearing the probe DNA decreased compared to that of the original aptamer; however, it recovered upon hybridization with the target DNA. Using this AES, we were able to detect target DNAs by measuring the thrombin activity in a homogeneous solution. Springer Netherlands 2007-09-12 2008 /pmc/articles/PMC7087721/ /pubmed/17849085 http://dx.doi.org/10.1007/s10529-007-9526-z Text en © Springer Science+Business Media B.V. 2007 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Original Research Paper
Ikebukuro, Kazunori
Yoshida, Wataru
Sode, Koji
Aptameric enzyme subunit for homogeneous DNA sensing
title Aptameric enzyme subunit for homogeneous DNA sensing
title_full Aptameric enzyme subunit for homogeneous DNA sensing
title_fullStr Aptameric enzyme subunit for homogeneous DNA sensing
title_full_unstemmed Aptameric enzyme subunit for homogeneous DNA sensing
title_short Aptameric enzyme subunit for homogeneous DNA sensing
title_sort aptameric enzyme subunit for homogeneous dna sensing
topic Original Research Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7087721/
https://www.ncbi.nlm.nih.gov/pubmed/17849085
http://dx.doi.org/10.1007/s10529-007-9526-z
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