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Inhibition of the mitochondrial Ca2+ uniporter by pure and impure ruthenium red
Authors:Kimberly M. Broekemeier  Randy J. Krebsbach  Douglas R. Pfeiffer
Affiliation:(1) Department of Medical Biochemistry, The Ohio State University, 1645 Neil Avenue, 310A Hamilton Hall, 43210-1218 Columbus, OH, USA;(2) The Hormel Institute, University of Minnesota, 55912-3698 Austin, MN, USA
Abstract:Commercial ruthenium red is often purified by a single recrystallization as described by Luft, J.H. (1971) Anat Rec 171, 347–368, which yields small amounts of material having an apparent molar extinction coefficient of sim67,400 at 533 nm. A simple modification to the procedure dramatically improves the yield, allowing crystallization to be repeated. Three times recrystallized ruthenium red has an apparent extinction coefficient of sim 85,900, the highest value reported to date. Both crude and highly purified ruthenium red can be shown to inhibit reverse activity of the mitochondrial Ca2+ uniporter (uncoupled mitochondria), provided that care is taken to minimize and account for Ca2+ release through the permeability transition pore. Crude ruthenium red is 7–10 fold more potent than the highly purified material in this regard, on an actual ruthenium red concentration basis. The same relative potency is seen against forward uniport (coupled mitochondria), however, the I50 values are 10 fold lower for both the crude and purified preparations. These data demonstrate unambiguously that the energy state of mitochondria affects the sensitivity of the Ca2+ uniporter to ruthenium red preparations, and that both the forward and reverse reactions are subject to complete inhibition. The data suggest, however, that the active inhibitor may not be ruthenium redper se, but one or more of the other ruthenium complexes which are present in ruthenium red preparations.Abbreviations CCP carbonyl cyanide p-chlorophenylhydrazone - CSA cyclosporin A - Hepes 4-(2-hydroxyethyl)-1-piperazine ethanesulfonic acid
Keywords:mitochondiral Ca2+ uniporter  ruthenium red  mitochondrial permeability transition  Ca2+ transport  cell Ca2+
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