The goal of this research is to develop surface enhanced Raman scattering (SERS) and surface enhanced resonance Raman scattering (SERRS) techniques for the study of biomolecules. During this funding period there are four specific aims. The first is to continue the development of new substrates for SERS/SERRS. This will include the use of Au and Cu as well as Ag in the form of electrodes, thin films, and coated spheres of known size distribution. The application of SERS to the study of chemically modified surfaces (especially SnO2 and carbon) will also be continued. Modification will be accomplished by spontaneous adsorption, deposition of Langmuir Blodgett monolayers, and covalent bonding.
The second aim i s to pursue SERS investigations of amino acids, proteins, and lipids on the above named metals, as well as the modified electrode surfaces. The objective is to identify specific interactions between these molecules and the electrode surfaces. The application of SERRS to mechanistic studies of electron transfer proteins constitutes the third aim. Methods for the evaluation of activity and structure in flavoenzymes and cytochrome c will be sought. New procedures for adsorbing these proteins to electrode surfaces will be attempted in an effort to preserve their native structure. A number of proteins containing chromosphores will also be examined by SERRS. These will include photosynthetic preparations, phytochrome, and phycocyanin. The goal of these studies is to utilize the surface sensitivity of SERRS to determine structural information about the proteins.
The fourth aim i s to pursue purely analytical applications of SERS/SERRS. This will include detection of proteins separated by chromatography. Methods for detecting the interaction of small chromophoric molecules with capture proteins will also be investigated. In all of the above studies, an effort will be made to increase the sensitivity of the surface Raman technique through the use of new experimental approaches (i.e. fiber optics, attenuated total reflectance and micro Raman sampling procedures). Advances in detector technology will also be important with respect to this goal.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
2R01GM035108-05
Application #
3287220
Study Section
Metallobiochemistry Study Section (BMT)
Project Start
1985-02-01
Project End
1993-03-31
Budget Start
1988-04-01
Budget End
1989-03-31
Support Year
5
Fiscal Year
1988
Total Cost
Indirect Cost
Name
University of Nebraska Lincoln
Department
Type
Schools of Arts and Sciences
DUNS #
555456995
City
Lincoln
State
NE
Country
United States
Zip Code
68588
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Zheng, J; Ye, S; Lu, T et al. (2000) Circular dichroism and resonance raman comparative studies of wild type cytochrome c and F82H mutant. Biopolymers 57:77-84
Hobara, D; Niki, K; Cotton, T M (1998) Effect of surface modifiers on the electrode reactions and conformation of cytochrome c3 adsorbed on a silver electrode. Biospectroscopy 4:161-70
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Raser, L N; Kolaczkowski, S V; Cotton, T M (1992) Resonance Raman and surface-enhanced resonance Raman spectroscopy of hypericin. Photochem Photobiol 56:157-62
Schlegel, V L; Cotton, T M (1991) Silver-island films as substrates for enhanced Raman scattering: effect of deposition rate on intensity. Anal Chem 63:241-7
Freund, M S; Brajter-Toth, A; Cotton, T M et al. (1991) Scanning tunneling microscopy and atomic force microscopy in the characterization of activated graphite electrodes. Anal Chem 63:1047-9
Chang, M C; Callahan, P M; Parkes-Loach, P S et al. (1990) Spectroscopic characterization of the light-harvesting complex of Rhodospirillum rubrum and its structural subunit. Biochemistry 29:421-9

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