By Rodney J. Devenish, Maria Galanis, Theo Papakonstantinou, Ruby H. P. Law (auth.), Prof. Dr. Sergio Papa, Prof. Dr. Angelo Azzi, Prof. Dr. Joseph M. Tager (eds.)
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Extra resources for Adenine Nucleotides in Cellular Energy Transfer and Signal Transduction
2 mM EDTA and 4 mM MgC1 2• At the used concentrations of nucleotides, the inhibition was maximal. 5 mM 8N3ADP 100 ~M NAP3 -ADP 100 ~M NAP~-2N~ADP INH. (%) 42 26 3 35 45 of Mg2+, the enzyme activity is partially inhibited (see Table III) . After a column centrifugation step the inhibition is still present and using radioactive ligands it could be established that about 2 moles of ligand remain bound per mole of enzyme. After addition of ATP one mole is exchanged and the other remains bound. With time the ligand slowly dissociates and the enzyme activity increases.
O 200 11,000 ', .... mgr1 ':". ,...... 500 . .... 1000 .... V (nmo! ATP·min"·mg") Fig. 1 Effect of attenuation of respiration rate and fractional inactivation of the ATP synthase complexes of SMP on the kinetics of ATP synthesis at 1-1,200 ~M ADP. The rate of ATP synthesis was measured at 30°C. ) or 30 mM DL-p-hydroxybutyrate plus 1 mM NAD (~). , the ATP synthase complexes of SMP were fractionally inactivated by incubating the particles with 20 ~M DCCD at OOC for 210 min. ). The inset shows apparent ~ and Vmax values at low (upper line) and high (lower line) _~embrane potential.
99, 1095-1100. J. (1991) Biochemistry 30, 5369-5378. B. (1984) Biochim. Biophys. Acta 768, 257-292. , & Hatefi, Y. (1984) Biochemistry A1, 5004-5009. Yoshida, M. (1983) Biochem. Biophys. Res. Commun. 114, 907-912. F. (1986) Biochemistry 25, 760-767. Adenine Nucleotides in Cellular Energy Transfer and Signal Transduction S. Papa, A. M. Tager (eds) © 1992 Birkhiiuser Verlag, BaseVSwitzeriand NUMBER, LOCALISATION AND FUNCTION OF THE NON-CATALYTIC ADENINE NUCLEOTIDE BINDING SITES OF MITOCHONDRIAL F,-ATPase Jan A.