Journal of Spectroscopy

Journal of Spectroscopy / 2010 / Article
Special Issue

From Molecule to Tissue: XIII European Conference on the Spectroscopy of Biological Molecules, Palermo, Italy, August 28–September 2, 2009, Part 1 of 2

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Volume 24 |Article ID 815817 |

Marc Grosserueschkamp, Christoph Nowak, Wolfgang Knoll, Renate L. C. Naumann, "Time-resolved surface-enhanced resonance Raman spectro-electrochemistry of heme proteins", Journal of Spectroscopy, vol. 24, Article ID 815817, 5 pages, 2010.

Time-resolved surface-enhanced resonance Raman spectro-electrochemistry of heme proteins


Heme proteins such as cytochrome c (cc) play a fundamental role in many biological processes. Surface-enhanced resonance Raman spectroscopy (SERRS) combined with electrochemical methods is an ideal tool to study the redox processes of heme proteins. In this context we designed a new measuring cell allowing for simultaneous electrochemical manipulation and high sensitive SERRS measurements of heme proteins. The measuring cell is based on an inverted rotating disc electrode for excitation by using a confocal Raman microscope. Furthermore, we developed a SER(R)S-active silver modified silver substrate for spectro-electrochemical applications. For this purpose silver nanoparticles (AgNPs) were adsorbed on top of a planar silver surface. The substrate was optimized for an excitation wavelength of 413 nm corresponding to the resonance frequency of heme structures. An enhancement factor of 105 was achieved. The high performance of the new measuring cell in combination with the new silver substrate was demonstrated using cc as a reference system.

Copyright © 2010 Hindawi Publishing Corporation. 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.

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