ENDOR electron-nuclear

In Chapter 2, ENDOR (electron-nuclear double resonance) was briefly described. To perform an ENDOR experiment it is necessary to apply both a radiofrequency and a microwave frequency, effectively performing simultaneous NMR and ESR, respectively, on the sample. The experiment is performed at a fixed magnetic field, with the ESR saturating frequency centered on a... 

The development of a wide range of special forms of EPR was initiated when the idea of double resonance (using simultaneous irradiation by two different sources) was cast in 1956 by G. Feher at Bell Telephone Labs in his seminal paper on ENDOR, electron nuclear double resonance (Feher 1956). BioEPR applications of ENDOR were later developed on flavoprotein radicals in a collaboration of A. Ehrenberg and L. E. G. Eriksson in Stockholm, Sweden, and J. S. Hyde at Varian in Palo Alto, California (Ehrenberg et al. 1968), and on metalloproteins in a joint effort of the groups of R. H. Sands in Ann Arbor, I. C. Gunsalus in Urbana, Illinois, and H. Beinert in Madison (Fritz et al. 1971). 

Double-resonance spectroscopy involves the use of two different sources of radiation. In the context of EPR, these usually are a microwave and a radiowave or (less common) a microwave and another microwave. The two combinations were originally called ENDOR (electron nuclear double resonance) and ELDOR (electron electron double resonance), but the development of many variations on this theme has led to a wide spectrum of derived techniques and associated acronyms, such as ESEEM (electron spin echo envelope modulation), which is a pulsed variant of ENDOR, or DEER (double electron electron spin resonance), which is a pulsed variant of ELDOR. The basic principle involves the saturation (partially or wholly) of an EPR absorption and the subsequent transfer of spin energy to a different absorption by means of the second radiation, leading to the detection of the difference signal. The requirement of saturability implies operation at close to liquid helium, or even lower, temperatures, which, combined with long experimentation times, produces a... 

ENDOR Electron Nuclear Double SCCC Self Consistence of Charge at... 

ENDOR (electron nuclear double resonance) studies of diphenyl-carbene indicated a dihedral angle of 34° for this species >. 

CW, continuous wave Cys, cysteine DFT, density functional theory ENDOR, electron nuclear double resonance ehba, 2-ethyl-2-hydroxybutanoate2 EPR, electron paramagnetic resonance Glc6P, D-glucose 6-phosphate GSH, reduced glutathione HEPES, 4-(2-hydroxyethyl)-l-piperazineethanesulfonic acid Hex, aldohexose ... 

The low-temperature EPR experiments used to determine the DNA ion radical distribution make it very clear that electron and hole transfer occurs after the initial random ionization. What then determines the final trapping sites of the initial ionization events To determine the final trapping sites, one must determine the protonation states of the radicals. This cannot be done in an ordinary EPR experiment since the small hyperfine couplings of the radicals only contribute to the EPR linewidth. However, detailed low-temperature EPR/ENDOR (electron nuclear double resonance) experiments can be used to determine the protonation states of the low-temperature products [17]. These proto-nation/deprotonation reactions are readily observed in irradiated single crystals of the DNA base constituents. The results of these experiments are that the positively charged radical cations tend to deprotonate and the negatively charged radical anions tend to protonate. 

ENDOR electron nuclear double resonance single unpaired electron/free radical)... 

ENDOR (Electron Nuclear Double Resonance) involves the simultaneous application of a microwave and a radio frequency signal to the sample. This is a technique invented by Feher in 1956. The original studies were on phosphorous-doped silicon. A description of the experimental results and apparatus used is presented in two Physical Review articles [24, 25], An excellent treatment of EPR double resonance techniques and theory is given in the book by Kevan and Kispert [26], What follows here is the theory and application of ENDOR used the in analysis of single crystal data with the goal of identifying free radical products in DNA constituents. 

Abbreviations AdoCbl, deoxyadenosylcobalamin AdoMet, S-adenosyl methionine dopa, 3,4-dihydroxyphenylalanine ENDOR, electron nuclear double resonance EPR, electron paramagnetic resonance NMR, nuclear magnetic resonance RNR, ribonucleotide reductase RTF, radical transfer pathway. 

PSII = Photosystem II WOC = Water-oxidizing complex OEC = Oxygen-evolving complex (B)RC = (Bacterial) Reaction Center Chi = Chlorophyll Bchl = Bacteriochloro-phyll XRD = X-ray diffraction EPR = Electron paramagnetic resonance EXAFS = Extended X-ray absorption fine stmctnre ENDOR = Electron-nuclear double resonance ESEEM = Electron spin echo envelope modulation (Tyr = Yz) = DlTyrl61 ATP = Adenosine Triphosphate KIE = Kinetic isotope effect UV = Ultraviolet (FT-)IR = (Fourier Transform) InfraRed. 

CoA = Coenzyme A CoM = Coenzyme M, 2-thioethane-sulfonate ENDOR = Electron nuclear double resonance EPR = Electron paramagnetic resonance H4MPT = Tetra-hydromethanopterin HS-HTP = N-7-mercaptoheptanoyl-O-phosphothreonine MCR = Methyl-CoM reductase MRF = Methyl-reducing factor XAS = X-ray absorption spectroscopy GSH = Glutathione. 

ENDOR = electron nuclear double resonance EPR = electron-paramagnetic resonance ESR = electron-spin resonance NMR = nuclear magnetic resonance MA = modulation amplitude SOFT = second-order perturbation theory s-o = spin-orbit zfs = zero-field splitting (for S > 1 /2) D = uniaxial zfs E = rhombic zfs g = g-factor with principal components gy, and g ge = free electron g-factor a = hyperfrne splitting constant A = hyperftne coupling constant for a given nucleus N (nuclear spin 7>0). 

DPPH = 2,2-diphenyl-1-picrylhydrazyl ENDOR= electron-nuclear double resonance EPR = electron paramagnetic resonance ESE = electron spin echoes ESEEM = electron spin echo envelope modulation EFT = fast fourier transformations FWHM = fidl width at half maximum HYSCORE = hyperfine sublevel correlation nqi = nuclear quadrupole interaction TauD = taurme/aKG dioxygenase TWTA = traveling wave tube amphfier ZFS = zero field sphtting. 

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