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Title: The synthesis of deuterium-substituted, spin-labeled analogues of AMP and NAD+ and their use in ESR studies of lactate dehydrogenase. Author: Glöggler KG, Balasubramanian K, Beth A, Fritzsche TM, Park JH, Pearson DE, Trommer WE, Venkastaramu SD. Journal: Biochim Biophys Acta; 1982 Feb 18; 701(2):224-8. PubMed ID: 6280769. Abstract: Two spin-labeled analogues of AMP and NAD+ were synthesized, in which a perdeuterated nitroxide radical (4-amino-2,2,6,6-tetramethylpiperidine-1-oxyl, TEMPAMINE) was attached to C-6 or C-8 position of the adenine ring. The ESR spectra of these derivatives exhibit a 4-fold increase in sensitivity and a concomitant decrease in line-width as compared to the corresponding protonated analogues. The improved resolution of composite spectra consisting of freely tumbling and immobilized components is demonstrated in ternary complexes of the spin-labeled NAD+ derivatives with lactate dehydrogenase (L-lactate:NAD+ oxidoreductase, EC 1.1.1.27) and oxalate.[Abstract] [Full Text] [Related] [New Search]