This application requests funds for continuation of support for an already existing Biotechnology Research Resource devoted to EPR spectroscopy. The pulsed EPR instrument was specifically designed for electron spin echo envelope modulation (ESEEM) studies of biological materials. Further, it is unique in that it has wide band capabilities, operating from 8-18 GHz, with proposed core development for operation in the 4-8 GHz range. Other core development of the Resource includes implementation of pulsed ENDOR spectroscopy as an alternative to conventional continuous wave (cw) methods so as to improve sensitivity in the study of magnetically dilute biological materials. A third aspect of core research is the study of single crystal protein samples as a means of defining in greater detail the electron nuclear coupling from individual groups or atoms in a protein structure. This will be applied to the examination of the blue copper proteins, with plastocyanin as an example, where preliminary ENDOR and ESEEM studies demonstrate inequivalence in electron nuclear coupling with the individual copper-coordinated imidazoles that constitute the metal binding site. Other core research will be devoted to the study of Mn(II)-17 0 interactions under exact cancellation conditions where the ESEEM spectrum is dominated by lines arising from nuclear quadrupolar interactions. The results of this study will be applied to the examination of metal substrate interactions with Mn(II)-enzymes. Finally, core research will be devoted to ESEEM studies of electron nuclear coupling to axial and in-plane nitrogen in various lowspin hemoproteins formed with exogenous and endogenous ligands. This project is made possible by the availability of 15N-substituted myoglobin and 15N-heme, so that all axial and equatorial ligands will be studied in the 14N-forms. A number of collaborative studies are proposed to identify and quantify the various metal coordinated ligands in various metalloproteins, the nature of nuclei interacting with free radical centers in biomolecules and the distance to deuterium in specifically labelled substrates and cofactors. LEFE studies are proposed to study the metal composition of iron sulfur clusters. Service and educational activities related to pulsed EPR as a probe of structure of paramagnetic biomolecules are proposed.

Agency
National Institute of Health (NIH)
Institute
National Center for Research Resources (NCRR)
Type
Biotechnology Resource Grants (P41)
Project #
3P41RR002583-13S1
Application #
6076703
Study Section
Special Emphasis Panel (ZRG7 (01))
Project Start
1985-09-30
Project End
2000-04-30
Budget Start
1998-05-05
Budget End
2000-04-30
Support Year
13
Fiscal Year
1999
Total Cost
Indirect Cost
Name
Albert Einstein College of Medicine
Department
Pharmacology
Type
Schools of Medicine
DUNS #
009095365
City
Bronx
State
NY
Country
United States
Zip Code
10461
Colaneri, M J; Vitali, J; Peisach, J (2000) Electron spin-echo envelope modulation study of multicrystalline Cu(2+)-insulin: effects of Cd(2+) on the nuclear quadrupole interaction of the Cu(2+)-coordinated imidazole remote nitrogen. Biochemistry 39:584-91
Lee, H C; Goroncy, A K; Peisach, J et al. (2000) Demonstration of a conserved histidine and two water ligands at the Mn2+ site in Diocleinae lectins by pulsed EPR spectroscopy. Biochemistry 39:2340-6
Sam, J W; Takahashi, S; Lippai, I et al. (1998) Sequence-specific changes in the metal site of ferric bleomycin induced by the binding of DNA. J Biol Chem 273:16090-7
Magliozzo, R S; Marcinkeviciene, J A (1997) The role of Mn(II)-peroxidase activity of mycobacterial catalase-peroxidase in activation of the antibiotic isoniazid. J Biol Chem 272:8867-70
Tipton, P A; Quinn, T P; Peisach, J et al. (1996) Role of the divalent metal ion in the NAD:malic enzyme reaction: an ESEEM determination of the ground state conformation of malate in the E:Mn:malate complex. Protein Sci 5:1648-54
Coffino, A R; Peisach, J (1996) Simulation of Mn (II) EPR spectra using a full spin-Hamiltonian approach. J Magn Reson B 111:127-34
Nersissian, A M; Mehrabian, Z B; Nalbandyan, R M et al. (1996) Cloning, expression, and spectroscopic characterization of Cucumis sativus stellacyanin in its nonglycosylated form. Protein Sci 5:2184-92
Gasdaska, J R; Law, J H; Bender, C J et al. (1996) Cockroach transferrin closely resembles vertebrate transferrins in its metal ion-binding properties: a spectroscopic study. J Inorg Biochem 64:247-58
Parast, C V; Wong, K K; Lewisch, S A et al. (1995) Hydrogen exchange of the glycyl radical of pyruvate formate-lyase is catalyzed by cysteine 419. Biochemistry 34:2393-9
Theodorakis, J L; Garber, E A; McCracken, J et al. (1995) A chemical modification of cytochrome-c lysines leading to changes in heme iron ligation. Biochim Biophys Acta 1252:103-13

Showing the most recent 10 out of 41 publications