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Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization

The adsorption and the redox behaviour of thrombin-binding aptamer (TBA) and extended TBA (eTBA) were studied using atomic force microscopy and voltammetry at highly oriented pyrolytic graphite and glassy carbon. The different adsorption patterns and degree of surface coverage were correlated with t...

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Autores principales: Diculescu, Victor Constantin, Chiorcea-Paquim, Ana-Maria, Eritja, Ramon, Oliveira-Brett, Ana Maria
Formato: Texto
Lenguaje:English
Publicado: SAGE-Hindawi Access to Research 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925381/
https://www.ncbi.nlm.nih.gov/pubmed/20798847
http://dx.doi.org/10.4061/2010/841932
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author Diculescu, Victor Constantin
Chiorcea-Paquim, Ana-Maria
Eritja, Ramon
Oliveira-Brett, Ana Maria
author_facet Diculescu, Victor Constantin
Chiorcea-Paquim, Ana-Maria
Eritja, Ramon
Oliveira-Brett, Ana Maria
author_sort Diculescu, Victor Constantin
collection PubMed
description The adsorption and the redox behaviour of thrombin-binding aptamer (TBA) and extended TBA (eTBA) were studied using atomic force microscopy and voltammetry at highly oriented pyrolytic graphite and glassy carbon. The different adsorption patterns and degree of surface coverage were correlated with the sequence base composition, presence/absence of K(+), and voltammetric behaviour of TBA and eTBA. In the presence of K(+), only a few single-stranded sequences present adsorption, while the majority of the molecules forms stable and rigid quadruplexes with no adsorption. Both TBA and eTBA are oxidized and the only anodic peak corresponds to guanine oxidation. Upon addition of K(+) ions, TBA and eTBA fold into a quadruplex, causing the decrease of guanine oxidation peak and occurrence of a new peak at a higher potential due to the oxidation of G-quartets. The higher oxidation potential of G-quartets is due to the greater difficulty of electron transfer from the inside of the quadruplex to the electrode surface than electron transfer from the more flexible single strands.
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spelling pubmed-29253812010-08-26 Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization Diculescu, Victor Constantin Chiorcea-Paquim, Ana-Maria Eritja, Ramon Oliveira-Brett, Ana Maria J Nucleic Acids Research Article The adsorption and the redox behaviour of thrombin-binding aptamer (TBA) and extended TBA (eTBA) were studied using atomic force microscopy and voltammetry at highly oriented pyrolytic graphite and glassy carbon. The different adsorption patterns and degree of surface coverage were correlated with the sequence base composition, presence/absence of K(+), and voltammetric behaviour of TBA and eTBA. In the presence of K(+), only a few single-stranded sequences present adsorption, while the majority of the molecules forms stable and rigid quadruplexes with no adsorption. Both TBA and eTBA are oxidized and the only anodic peak corresponds to guanine oxidation. Upon addition of K(+) ions, TBA and eTBA fold into a quadruplex, causing the decrease of guanine oxidation peak and occurrence of a new peak at a higher potential due to the oxidation of G-quartets. The higher oxidation potential of G-quartets is due to the greater difficulty of electron transfer from the inside of the quadruplex to the electrode surface than electron transfer from the more flexible single strands. SAGE-Hindawi Access to Research 2010-06-16 /pmc/articles/PMC2925381/ /pubmed/20798847 http://dx.doi.org/10.4061/2010/841932 Text en Copyright © 2010 Victor Constantin Diculescu et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Diculescu, Victor Constantin
Chiorcea-Paquim, Ana-Maria
Eritja, Ramon
Oliveira-Brett, Ana Maria
Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization
title Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization
title_full Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization
title_fullStr Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization
title_full_unstemmed Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization
title_short Thrombin-Binding Aptamer Quadruplex Formation: AFM and Voltammetric Characterization
title_sort thrombin-binding aptamer quadruplex formation: afm and voltammetric characterization
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2925381/
https://www.ncbi.nlm.nih.gov/pubmed/20798847
http://dx.doi.org/10.4061/2010/841932
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