Issue 10, 2016

Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion

Abstract

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 N2H4 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.

Graphical abstract: Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion

Supplementary files

Article information

Article type
Edge Article
Submitted
16 May 2016
Accepted
22 Jun 2016
First published
01 Jul 2016
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2016,7, 6450-6457

Electrocatalytic amplification of DNA-modified nanoparticle collisions via enzymatic digestion

A. D. Castañeda, D. A. Robinson, K. J. Stevenson and R. M. Crooks, Chem. Sci., 2016, 7, 6450 DOI: 10.1039/C6SC02165D

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