Real-time surface-enhanced Raman spectroscopy monitoring of surface pH during electrochemical melting of double-stranded DNA
Real-time surface-enhanced Raman spectroscopy monitoring of surface pH during electrochemical melting of double-stranded DNA
The application of a negative potential ramp at a double-stranded DNA (dsDNA) functionalized electrode surface results in the gradual denaturation of the DNA in a process known as electrochemical melting. The underlying physical chemistry behind electrochemically driven DNA denaturation is not well understood, and one possible mechanism is a change in local pH at the electrode surface. We demonstrate that by coimmobilization of p-mercaptobenozic acid at a dsDNA-functionalized electrode surface, it is possible to monitor both DNA denaturation and the local pH simultaneously using surface-enhanced Raman spectroscopy. We find that the local pH at the electrode surface does not change as the applied potential is scanned negative and the dsDNA denatures. We therefore conclude that in these experiments electrochemical melting is not caused by electrochemically driven local pH changes.
5464-5470
Johnson, Robert P.
5dabdb76-784a-4d20-bed7-447f2a42705b
Richardson, James
51db9f73-a136-48af-8722-21d46906cf40
Brown, Tom
a64aae36-bb30-42df-88a2-11be394e8c89
Bartlett, Philip N.
d99446db-a59d-4f89-96eb-f64b5d8bb075
2012
Johnson, Robert P.
5dabdb76-784a-4d20-bed7-447f2a42705b
Richardson, James
51db9f73-a136-48af-8722-21d46906cf40
Brown, Tom
a64aae36-bb30-42df-88a2-11be394e8c89
Bartlett, Philip N.
d99446db-a59d-4f89-96eb-f64b5d8bb075
Johnson, Robert P., Richardson, James, Brown, Tom and Bartlett, Philip N.
(2012)
Real-time surface-enhanced Raman spectroscopy monitoring of surface pH during electrochemical melting of double-stranded DNA.
Langmuir, 28 (12), .
(doi:10.1021/la204794g).
Abstract
The application of a negative potential ramp at a double-stranded DNA (dsDNA) functionalized electrode surface results in the gradual denaturation of the DNA in a process known as electrochemical melting. The underlying physical chemistry behind electrochemically driven DNA denaturation is not well understood, and one possible mechanism is a change in local pH at the electrode surface. We demonstrate that by coimmobilization of p-mercaptobenozic acid at a dsDNA-functionalized electrode surface, it is possible to monitor both DNA denaturation and the local pH simultaneously using surface-enhanced Raman spectroscopy. We find that the local pH at the electrode surface does not change as the applied potential is scanned negative and the dsDNA denatures. We therefore conclude that in these experiments electrochemical melting is not caused by electrochemically driven local pH changes.
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e-pub ahead of print date: 27 February 2012
Published date: 2012
Organisations:
Electrochemistry
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Local EPrints ID: 349749
URI: http://eprints.soton.ac.uk/id/eprint/349749
ISSN: 0743-7463
PURE UUID: 053ad3cf-7d5e-4f58-9952-3917f2570c68
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Date deposited: 08 Mar 2013 18:02
Last modified: 15 Mar 2024 02:44
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Author:
Robert P. Johnson
Author:
James Richardson
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