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Utilization of heavy-atom effect quenching of pyrene fluorescence to determine the intramembrane distribution of halothane
Authors:K Washington  M M Sarasua  L S Koehler  K A Koehler  J A Schultz  L G Pedersen  R G Hiskey
Institution:Chemistry Department, University of North Carolina, Chapel Hill, NC 27514, USA;Departments of Pharmaceutical Science and Psychiatry, Medical University of South Carolina, 171 Ashley Ave., Charleston, SC 29425, USA;Cleveland Clinic Foundation, Department of Cardio-Thoracic Anesthesiology, 9500 Euclid Avenue, Cleveland, OH 44106, USA.;Departments of Surgery and Biochemistry, Case Western Reserve University, Cleveland Metropolitan General Hospital, 3395 Scranton Road, Cleveland, OH 44109, USA
Abstract:The interaction of halothane (CF3CHBrCl) with dipalmitoylphosphatidylcholine (DPPC) membranes containing varying amounts of dipalmitoylphosphatidylglycerol (DPPG) was examined via heavy atom effect quenching of pyrene fluorescence by halothane. The effect of halothane on pyrene fluorescence is consistent with a kinetic model based upon the assumption of the existence of two populations of pyrene in the membrane: one accessible to interactions with halothane; the second inaccessible to halothane on the time scale of the pyrene fluorescence excited state. Both populations of pyrene are affected by the presence of halothane in the membrane. The rate of halothane quenching of pyrene fluorescence is increased significantly for all DPPG/DPPC membranes compared to pure DPPC membranes indicating that any DPPG in the membrane facilitates interaction between halothane and pyrene even though the measured partition coefficients indicate that little change in total halothane concentration in the membrane as a whole occurs as a function of percent DPPG in DPPG/DPPC mixtures.
It is speculated that phase boundaries play an important role in determining the behavior of this model system by determining the location of the pyrene probe. The heavy atom effect quenching of pyrene by halothane provides a useful probe of phase boundaries in membranes.
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