GM22923 is concerned with development of nitroxide radical """"""""spin-label"""""""" electron spin resonance (ESR) methodology. In this competitive renewal for years -14 to -18, focus is on measurements of bimolecular collision rates between (a) spin labels and molecular oxygen (so-called spin-label oximetry), (b) between spin labels and organo-metallic complexes and (c) between spin-labeled biomolecules that contain the 14N isotope and those that contain the 15N isotope. The experiments are based on pulse ESR techniques and computer deconvolution of the resulting multiexponential saturation-recovery signals as developed in the previous funding period. Engineering refinements of the existing high speed signal acquisition equipment are proposed in order to minimize instrumental distortion of transient signals. Essentially all experiments involve synthetic lipid bilayerrs and biological membranes. Most previous spin- label experiments in membranes were concerned with rotational processes, but translational processes studied here through the measurement of bimolecular collision rates are felt to be more biologically relevant. A method has been devised to determine for the first time the oxygen permeability of a membrane. Oxygen transport across the membrane is crucial to cellular respiration. In other studies, rate consants for physical exchange between lipids in two environments in heterogeneous membraneous systems will be measured. Further development of """"""""multifrequency saturation- recovery"""""""" equipment will be carried out: namely, construction of a K-band pulse accessory to supplement existing X-band and """"""""under-construction"""""""" S- band pulse equipment. Multifrequency saturation-recovery capability will be useful for two purposes: (1) measurement of dipolar non-secular contributtions to spin-label relaxation in fluids, which will improve the quality of the data on bimolecular collisions (this information arises primarily from Heisenberg exchange, but can be confounded by dipolar contributions), and (2) measurement of distances of closest approach between spin labels in membranes and metal ions on the membran surface. A considerable amount of organic synthesis of novel spin labels, organo- metallic compounds and 15 N- substituted spin labels is proposed including synthesis of phospholipids with metal-ion chelation groups attached to the phosphate groups. This is an interdisciplinary program involving physicists, biochemists, biophysicists, chemists, and engineers at the National Biomedical ESR Center.

Agency
National Institute of Health (NIH)
Institute
National Institute of General Medical Sciences (NIGMS)
Type
Method to Extend Research in Time (MERIT) Award (R37)
Project #
5R37GM022923-17
Application #
3484437
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1979-03-01
Project End
1994-02-28
Budget Start
1992-03-01
Budget End
1993-02-28
Support Year
17
Fiscal Year
1992
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
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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
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
Ligeza, A; Tikhonov, A N; Hyde, J S et al. (1998) Oxygen permeability of thylakoid membranes: electron paramagnetic resonance spin labeling study. Biochim Biophys Acta 1365:453-63

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