Correction for inner filter effects in turbid samples: fluorescence assays of mitochondrial NADH.

Fluorescent determinations of NADH in porcine heart mitochondria were subject to significant errors caused by alterations in inner filter effects during numerous metabolic perturbations. These inner filter effects were primarily associated with changes in mitochondrial volume and accompanying light scattering. The observed effects were detected in a standard commercial fluorometer with emission orthogonal to the excitation light path and, to a lesser extent, in a light path geometry detecting only the surface fluorescence. A method was developed to detect and correct for inner filter effects on mitochondrial NADH fluorescence measurements that were independent of the optical path geometry using an internal fluorescent standard and linear least-squares spectral analysis. A simple linear correction with the inner fluorescence reference was found to adequately correct for inner filter effects. This approach may be useful for other fluorescence probes in isolated mitochondria or other light-scattering media.

[1]  B CHANCE,et al.  Respiratory enzymes in oxidative phosphorylation. VII. Binding of intramitochondrial reduced pyridine nucleotide. , 1958, The Journal of biological chemistry.

[2]  A. Beavis,et al.  Swelling and contraction of the mitochondrial matrix. I. A structural interpretation of the relationship between light scattering and matrix volume. , 1985, The Journal of biological chemistry.

[3]  B. Schoener,et al.  Intracellular Oxidation-Reduction States in Vivo , 1962, Science.

[4]  H. Krebs,et al.  The redox state of free nicotinamide-adenine dinucleotide in the cytoplasm and mitochondria of rat liver. , 1967, The Biochemical journal.

[5]  D. Webb,et al.  Photoluminescence of solutions , 1969 .

[6]  W. Bartley,et al.  The swelling and contraction of isolated rat-liver mitochondria. , 1964, The Biochemical journal.

[7]  A. Fabiato,et al.  Calculator programs for computing the composition of the solutions containing multiple metals and ligands used for experiments in skinned muscle cells. , 1979, Journal de physiologie.

[8]  R. Estabrook,et al.  A POSSIBLE ROLE FOR PYRIDINE NUCLEOTIDE IN COUPLING MECHANISM OF OXIDATIVE PHOSPHORYLATION. , 1963, Federation proceedings.

[9]  Z. Kam,et al.  Absorption and Scattering of Light by Small Particles , 1998 .

[10]  K. Tanaka,et al.  Spectrophotometric determination of oxidized and reduced pyridine nucleotides in erythrocytes using a single extraction procedure. , 1987, Analytical biochemistry.

[11]  R. Estabrook,et al.  Fluorometric measurement of reduced pyridine nucleotide in cellular and subcellular particles. , 1962, Analytical biochemistry.

[12]  R S Balaban,et al.  Nmr spectral analysis of kinetic data using natural lineshapes , 1990, Magnetic resonance in medicine.

[13]  S. Fleischer,et al.  Mitochondrial D- -hydroxybutyrate dehydrogenase. 3. Isolation and characterization. , 1973, The Journal of biological chemistry.

[14]  A. Panov,et al.  Substrate specific effects of calcium on metabolism of rat heart mitochondria. , 1996, The American journal of physiology.

[15]  A. Halestrap The regulation of the matrix volume of mammalian mitochondria in vivo and in vitro and its role in the control of mitochondrial metabolism. , 1989, Biochimica et biophysica acta.

[16]  T. E. Thompson,et al.  ANGULAR LIGHT-SCATTERING STUDIES ON ISOLATED MITOCHONDRIA , 1961, The Journal of biophysical and biochemical cytology.

[17]  V. Mootha,et al.  Maximum oxidative phosphorylation capacity of the mammalian heart. , 1997, The American journal of physiology.

[18]  R S Balaban,et al.  Spectroscopic determination of cytochrome c oxidase content in tissues containing myoglobin or hemoglobin. , 1996, Analytical biochemistry.

[19]  R. Balaban,et al.  Metabolic substrate utilization by rabbit proximal tubule. An NADH fluorescence study. , 1988, The American journal of physiology.

[20]  A. Koretsky,et al.  Determination of pyridine nucleotide fluorescence from the perfused heart using an internal standard. , 1987, The American journal of physiology.

[21]  A. Beavis,et al.  Swelling and contraction of the mitochondrial matrix. II. Quantitative application of the light scattering technique to solute transport across the inner membrane. , 1985, The Journal of biological chemistry.

[22]  E. Rabinowitch,et al.  Selective scattering of light by pigments in vivo. , 1959, Archives of biochemistry and biophysics.

[23]  M. Rigoulet,et al.  Dependence of flux size and efficiency of oxidative phosphorylation on external osmolarity in isolated rat liver mitochondria: role of adenine nucleotide carrier. , 1996, Biochimica et biophysica acta.

[24]  Robert D. Pearlstein,et al.  Cerebral cortical microfluorometry at isosbestic wavelengths for correction of vascular artifact. , 1979, Science.

[25]  A. Lehninger Reversal of various types of mitochondrial swelling by adenosine triphosphate. , 1959, The Journal of biological chemistry.

[26]  R. Balaban,et al.  Fluorescence emission spectroscopy of 1,4-dihydroxyphthalonitrile. A method for determining intracellular pH in cultured cells. , 1985, Biophysical journal.

[27]  L. Geren,et al.  Fluorescence energy transfer studies of the interaction between adrenodoxin and cytochrome c. , 1981, The Journal of biological chemistry.

[28]  M. Tamura,et al.  Some characteristics of the fluorescence lifetime of reduced pyridine nucleotides in isolated mitochondria, isolated hepatocytes, and perfused rat liver in situ. , 1995, Journal of biochemistry.

[29]  B. Chance,et al.  Intracellular Oxidation-Reduction States in Vivo , 1962, Science.

[30]  R S Balaban,et al.  Nicotinamide adenine dinucleotide fluorescence spectroscopy and imaging of isolated cardiac myocytes. , 1989, Biophysical journal.

[31]  A. Koretsky,et al.  Changes in pyridine nucleotide levels alter oxygen consumption and extra-mitochondrial phosphates in isolated mitochondria: a 31P-NMR and NAD(P)H fluorescence study. , 1987, Biochimica et biophysica acta.