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Scanning Electrochemical Microscopy of DNA Monolayers Modified with Nile Blue

Gorodetsky, Alon A. and Hammond, William J. and Hill, Michael G. and Slowinski, Krzysztof and Barton, Jacqueline K. (2008) Scanning Electrochemical Microscopy of DNA Monolayers Modified with Nile Blue. Langmuir, 24 (24). pp. 14282-14288. ISSN 0743-7463. PMCID PMC2668266. doi:10.1021/la8029243.

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Scanning electrochemical microscopy (SECM) is used to probe long-range charge transport (CT) through DNA monolayers containing the redox-active Nile Blue (NB) intercalator covalently affixed at a specific location in the DNA film. At substrate potentials negative of the formal potential of covalently attached NB, the electrocatalytic reduction of Fe(CN)63− generated at the SECM tip is observed only when NB is located at the DNA/solution interface; for DNA films containing NB in close proximity to the DNA/electrode interface, the electrocatalytic effect is absent. This behavior is consistent with both rapid DNA-mediated CT between the NB intercalator and the gold electrode as well as a rate-limiting electron transfer between NB and the solution phase Fe(CN)63−. The DNA-mediated nature of the catalytic cycle is confirmed through sequence-specific and localized detection of attomoles of TATA-binding protein, a transcription factor that severely distorts DNA upon binding. Importantly, the strategy outlined here is general and allows for the local investigation of the surface characteristics of DNA monolayers both in the absence and in the presence of DNA binding proteins. These experiments highlight the utility of DNA-modified electrodes as versatile platforms for SECM detection schemes that take advantage of CT mediated by the DNA base pair stack.

Item Type:Article
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URLURL TypeDescription CentralArticle
Gorodetsky, Alon A.0000-0002-3811-552X
Barton, Jacqueline K.0000-0001-9883-1600
Additional Information:Copyright © 2008 American Chemical Society. Received September 5, 2008. Revised Manuscript Received October 13, 2008. Publication Date (Web): November 21, 2008. We are grateful to the NIH (GM61077 to J.K.B.) and the ACS-PRF (to K.S. and M.G.H.) for their financial support of this research. These authors [AAG and WJH] contributed equally to this work. Supporting Information: Structure of the NB-modified uridine. Cyclic voltammetry and plots of peak current as a function of scan rate for DNA monolayers modified with NB at both the top and the bottom. Cyclic voltammetry of ferricyanide at a bare and a mercaptoundecylphosphoric acid-modified gold electrode. SECM approach curves for a DNA monolayer modified with NB at the bottom in the presence and absence of MB. This material is available free of charge via the Internet at
Funding AgencyGrant Number
American Chemical Society Petroleum Research FundUNSPECIFIED
Issue or Number:24
PubMed Central ID:PMC2668266
Record Number:CaltechAUTHORS:GORl08
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Official Citation:Scanning Electrochemical Microscopy of DNA Monolayers Modified with Nile Blue Alon A. Gorodetsky, William J. Hammond, Michael G. Hill, Krzysztof Slowinski, and Jacqueline K. Barton Langmuir 2008 24 (24), 14282-14288 DOI: 10.1021/la8029243
Usage Policy:No commercial reproduction, distribution, display or performance rights in this work are provided.
ID Code:12919
Deposited By: Archive Administrator
Deposited On:11 Jan 2009 04:02
Last Modified:08 Nov 2021 22:33

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