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Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion

We report a new and general approach that will be useful for adapting the method of electrocatalytic amplification (ECA) to biosensing applications. In ECA, individual collisions of catalytic nanoparticles with a noncatalytic electrode surface lead to bursts of current. In the work described here, t...

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Detalles Bibliográficos
Autores principales: Castañeda, Alma D., Robinson, Donald A., Stevenson, Keith J., Crooks, Richard M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356041/
https://www.ncbi.nlm.nih.gov/pubmed/28451102
http://dx.doi.org/10.1039/c6sc02165d
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author Castañeda, Alma D.
Robinson, Donald A.
Stevenson, Keith J.
Crooks, Richard M.
author_facet Castañeda, Alma D.
Robinson, Donald A.
Stevenson, Keith J.
Crooks, Richard M.
author_sort Castañeda, Alma D.
collection PubMed
description We report a new and general approach that will be useful for adapting the method of electrocatalytic amplification (ECA) to biosensing applications. In ECA, individual collisions of catalytic nanoparticles with a noncatalytic electrode surface lead to bursts of current. In the work described here, the current arises from catalytic electrooxidation of N(2)H(4) at the surface of platinum nanoparticles (PtNPs). The problem with using ECA for biosensing applications heretofore, is that it is necessary to immobilize a receptor, such as DNA (as in the case here) or an antibody on the PtNP surface. This inactivates the colliding NP, however, and leads to very small collision signatures. In the present article, we show that single-stranded DNA (ssDNA) present on the PtNP surface can be detected by selectively removing a fraction of the ssDNA using the enzyme Exonuclease I (Exo I). About half of the current associated with collisions of naked PtNPs can be recovered from fully passivated PtNPs after exposure to Exo I. Experiments carried out using both Au and Hg ultramicroelectrodes reveal some mechanistic aspects of the collision process before and after treatment of the ssDNA-modified PtNPs with Exo I.
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spelling pubmed-53560412017-04-27 Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion Castañeda, Alma D. Robinson, Donald A. Stevenson, Keith J. Crooks, Richard M. Chem Sci Chemistry We report a new and general approach that will be useful for adapting the method of electrocatalytic amplification (ECA) to biosensing applications. In ECA, individual collisions of catalytic nanoparticles with a noncatalytic electrode surface lead to bursts of current. In the work described here, the current arises from catalytic electrooxidation of N(2)H(4) at the surface of platinum nanoparticles (PtNPs). The problem with using ECA for biosensing applications heretofore, is that it is necessary to immobilize a receptor, such as DNA (as in the case here) or an antibody on the PtNP surface. This inactivates the colliding NP, however, and leads to very small collision signatures. In the present article, we show that single-stranded DNA (ssDNA) present on the PtNP surface can be detected by selectively removing a fraction of the ssDNA using the enzyme Exonuclease I (Exo I). About half of the current associated with collisions of naked PtNPs can be recovered from fully passivated PtNPs after exposure to Exo I. Experiments carried out using both Au and Hg ultramicroelectrodes reveal some mechanistic aspects of the collision process before and after treatment of the ssDNA-modified PtNPs with Exo I. Royal Society of Chemistry 2016-10-01 2016-07-01 /pmc/articles/PMC5356041/ /pubmed/28451102 http://dx.doi.org/10.1039/c6sc02165d Text en This journal is © The Royal Society of Chemistry 2016 http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial 3.0 Unported License (http://creativecommons.org/licenses/by-nc/3.0/) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Chemistry
Castañeda, Alma D.
Robinson, Donald A.
Stevenson, Keith J.
Crooks, Richard M.
Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion
title Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion
title_full Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion
title_fullStr Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion
title_full_unstemmed Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion
title_short Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion
title_sort electrocatalytic amplification of dna-modified nanoparticle collisions via enzymatic digestion
topic Chemistry
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5356041/
https://www.ncbi.nlm.nih.gov/pubmed/28451102
http://dx.doi.org/10.1039/c6sc02165d
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