The purpose of this research is to develop methodology that enchances the usefulness of nitroxide radical spin-labels as probes of structure and function of biological systems using electron paramagnetic resonance (EPR) spectroscopy. The proposal contains two main subject areas: saturation transfer spectroscopy and spin-label oximetry, these being the subjects of greatest significane in research under this grant in the preceding eight years. In saturation transfer, five new experimental methods are proposed - with intensive applications to measurements of motion and transport in liposomal and cellular membranes. A particularly novel experiment involves electron-electron double resonance (ELDOR) between 14N and 15N substituted spin labels, thereby permitting a direct measurement of the collision frequency between labels in different parts of the membrane. Many of the saturation transfer experiments involve time domain or pulse EPR. The second subject area, spin-label oximetry, is primarily concerned with studies of cellular respiration based on measurement of collisions between oxygen and spin-labels. Experiments are proposed to determine the role of diffusion limitation in respiration, which is thought to be critical in oxygen depleted regions of solid tumors. Also, for the first time it is believed, a way has been found to measure the enthalpy and entropy of repiration -- fundamental thermodynamic quantities that contribute to our understanding of the respiratory process at the most basic level. Related grants held by the P.I.: National Biomedial ESR Center (RR01008) and Development of Biomedical ESR Instrumentation (GM27665) provide funds for the development of new ESR instruments used in some of the research of the present proposal and make all instrumental and methodological advances available at a national level.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Research Project (R01)
Project #
5R01GM022923-10
Application #
3271404
Study Section
Biophysics and Biophysical Chemistry B Study Section (BBCB)
Project Start
1979-03-01
Project End
1989-02-28
Budget Start
1985-03-01
Budget End
1986-02-28
Support Year
10
Fiscal Year
1985
Total Cost
Indirect Cost
Name
Medical College of Wisconsin
Department
Type
Schools of Medicine
DUNS #
073134603
City
Milwaukee
State
WI
Country
United States
Zip Code
53226
Kawasaki, K; Yin, J J; Subczynski, W K et al. (2001) Pulse EPR detection of lipid exchange between protein-rich raft and bulk domains in the membrane: methodology development and its application to studies of influenza viral membrane. Biophys J 80:738-48
Singh, R J; Hogg, N; Joseph, J et al. (1999) The peroxynitrite generator, SIN-1, becomes a nitric oxide donor in the presence of electron acceptors. Arch Biochem Biophys 361:331-9
Koteiche, H A; Mchaourab, H S (1999) Folding pattern of the alpha-crystallin domain in alphaA-crystallin determined by site-directed spin labeling. J Mol Biol 294:561-77
Hogg, N; Kalyanaraman, B (1999) Nitric oxide and lipid peroxidation. Biochim Biophys Acta 1411:378-84
Klug, C S; Feix, J B (1998) Guanidine hydrochloride unfolding of a transmembrane beta-strand in FepA using site-directed spin labeling. Protein Sci 7:1469-76
Wisniewska, A; Subczynski, W K (1998) Effects of polar carotenoids on the shape of the hydrophobic barrier of phospholipid bilayers. Biochim Biophys Acta 1368:235-46
Pezeshk, A; Wojas, J; Subczynski, W K (1998) Partitioning and structural effects of the antitumor drug daunomycin on model membranes. Life Sci 63:1863-70
Koteiche, H A; Berengian, A R; Mchaourab, H S (1998) Identification of protein folding patterns using site-directed spin labeling. Structural characterization of a beta-sheet and putative substrate binding regions in the conserved domain of alpha A-crystallin. Biochemistry 37:12681-8
Subczynski, W K; Hyde, J S (1998) Membranes. Barriers or pathways for oxygen transport. Adv Exp Med Biol 454:399-408
Singh, R J; Goss, S P; Joseph, J et al. (1998) Nitration of gamma-tocopherol and oxidation of alpha-tocopherol by copper-zinc superoxide dismutase/H2O2/NO2-: role of nitrogen dioxide free radical. Proc Natl Acad Sci U S A 95:12912-7

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