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 #
5R37GM022923-18
Application #
3484438
Study Section
Biophysical Chemistry Study Section (BBCB)
Project Start
1979-03-01
Project End
1994-02-28
Budget Start
1993-03-01
Budget End
1994-02-28
Support Year
18
Fiscal Year
1993
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; Eaton, S S; Eaton, G R et al. (1998) Ligand-induced conformational change in the ferric enterobactin receptor FepA as studied by site-directed spin labeling and time-domain ESR. Biochemistry 37:9016-23
Singh, R J; Karoui, H; Gunther, M R et al. (1998) Reexamination of the mechanism of hydroxyl radical adducts formed from the reaction between familial amyotrophic lateral sclerosis-associated Cu,Zn superoxide dismutase mutants and H2O2. Proc Natl Acad Sci U S A 95:6675-80
Subczynski, W K; Lewis, R N; McElhaney, R N et al. (1998) Molecular organization and dynamics of 1-palmitoyl-2-oleoylphosphatidylcholine bilayers containing a transmembrane alpha-helical peptide. Biochemistry 37:3156-64
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

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