Determination of the Oligomeric States of Human and Rat Monoamine Oxidases in the Outer Mitochondrial Membrane and Octyl β-d-Glucopyranoside Micelles Using Pulsed Dipolar Electron Spin Resonance Spectroscopy†

Biochemistry ◽  
2008 ◽  
Vol 47 (6) ◽  
pp. 1554-1566 ◽  
Author(s):  
Anup K. Upadhyay ◽  
Peter P. Borbat ◽  
Jin Wang ◽  
Jack H. Freed ◽  
Dale E. Edmondson
Keyword(s):  
Electron Spin Resonance ◽  
Electron Spin ◽  
Mitochondrial Membrane ◽  
Electron Spin Resonance Spectroscopy ◽  
Resonance Spectroscopy ◽  
Outer Mitochondrial Membrane ◽  
Monoamine Oxidases ◽  
Spin Resonance

Determination of Thermal Histories of Archeological Cereal Grains with Electron Spin Resonance Spectroscopy

Science ◽  
1983 ◽  
Vol 222 (4629) ◽  
pp. 1235-1236 ◽  
Author(s):  
G. C. HILLMAN ◽  
G. V. ROBINS ◽  
D. ODUWOLE ◽  
K. D. SALES ◽  
D. A. C. MCNEIL
Keyword(s):  
Electron Spin Resonance ◽  
Electron Spin ◽  
Cereal Grains ◽  
Electron Spin Resonance Spectroscopy ◽  
Resonance Spectroscopy ◽  
Spin Resonance ◽  
Thermal Histories

Determination of the Rates of Ring-Closure of Oxygen-Containing Analogs of Hex-5-Enyl Radical by Kinetic Electron Spin Resonance Spectroscopy

1987 ◽  
Vol 40 (1) ◽  
pp. 157 ◽  
Author(s):  
ALJ Beckwith ◽  
SA Glover
Keyword(s):  
Electron Spin Resonance ◽  
Electron Spin ◽  
Activation Parameters ◽  
Ring Closure ◽  
Electron Spin Resonance Spectroscopy ◽  
Resonance Spectroscopy ◽  
Restricted Rotation ◽  
Conformational Effects ◽  
Spin Resonance

The hex-5-enyl (1), 3-oxahex-5-enyl (6), 2-oxahex-5-enyl (9) and 2,2-dimethylbut-3- enoyloxymethyl (13) radicals have been generated by interaction of the corresponding bromides with trialkyltin or trialkylgermanium radicals, and their rate constants and activation parameters for cyclization have been determined by kinetic e.s.r . spectroscopy. The 3-oxa species (6) undergo 1,5-ring closure more rapidly than does hex-5-enyl radical (1) because of favourable stereoelectronic factors. Spectral evidence has been obtained for restricted rotation about the O-CH2* bond in the 2-oxa radical (9) as a consequence of which its ring closure is relatively slow. Similarly, 1,5-ring closure of the ester derived radical (13) is slow because of unfavourable conformational effects arising from restricted rotation about the CO-O bond. The radical (22) formed from allyl bromoacetate does not undergo ring closure. Spectral data have been obtained for various radicals (16), (19), (23), (24) formed by intermolecular addition.

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