Concentration of NADH-cytochrome b5 reductase in erythrocytes of normal and methemoglobinemic individuals measured with a quantitative radioimmunoblotting assay.

The activity of NADH-cytochrome b5 reductase (NADH-methemoglobin reductase) is generally reduced in red cells of patients with recessive hereditary methemoglobinemia. To determine whether this lower activity is due to reduced concentration of an enzyme with normal catalytic properties or to reduced activity of an enzyme present at normal concentration, we measured erythrocyte reductase concentrations with a quantitative radioimmunoblotting method, using affinity-purified polyclonal antibodies against rat liver microsomal reductase as probe. In five patients with the "mild" form of recessive hereditary methemoglobinemia, in which the activity of erythrocyte reductase was 4-13% of controls, concentrations of the enzyme, measured as antigen, were also reduced to 7-20% of the control values. The concentration of membrane-bound reductase antigen, measured in the ghost fraction, was similarly reduced. Thus, in these patients, the reductase deficit is caused mainly by a reduction in NADH-cytochrome b5 reductase concentration, although altered catalytic properties of the enzyme may also contribute to the reduced enzyme activity.

[1]  N. Borgese,et al.  Distribution of the integral membrane protein NADH-cytochrome b5 reductase in rat liver cells, studied with a quantitative radioimmunoblotting assay. , 1986, The Biochemical journal.

[2]  A. Tomoda,et al.  Hereditary methemoglobinemia due to cytochrome b5 reductase deficiency in blood cells without associated neurologic and mental disorders , 1985 .

[3]  G. Korza,et al.  Complete amino acid sequence of steer liver microsomal NADH-cytochrome b5 reductase. , 1985, The Journal of biological chemistry.

[4]  S. Iwanaga,et al.  Amino acid sequence of NADH-cytochrome b5 reductase of human erythrocytes. , 1984, Journal of Biochemistry (Tokyo).

[5]  E. Beutler Selectivity of proteases as a basis for tissue distribution of enzymes in hereditary deficiencies. , 1983, Proceedings of the National Academy of Sciences of the United States of America.

[6]  M. Tamura,et al.  Exponential decay of cytochrome b5 and cytochrome b5 reductase during senescence of erythrocytes: relation to the increased methemoglobin content. , 1983, Journal of biochemistry.

[7]  N. Borgese,et al.  Rat erythrocyte NADH-cytochrome b5 reductase. Quantitation and comparison between the membrane-bound and soluble forms using an antibody against the rat liver enzyme. , 1982, The Journal of biological chemistry.

[8]  J. Wilson,et al.  Human hypoxanthine-guanine phosphoribosyltransferase. Purification and characterization of mutant forms of the enzyme. , 1981, The Journal of biological chemistry.

[9]  Y. Yasukochi,et al.  Purification and properties of human erythrocyte membrane NADH-cytochrome b5 reductase. , 1981, Archives of biochemistry and biophysics.

[10]  T. Matsuki,et al.  Age-dependent decay of cytochrome b5 and cytochrome b5 reductase in human erythrocytes. , 1981, The Biochemical journal.

[11]  C. Junien,et al.  [Prenatal diagnosis of generalized cytochrome b5 reductase deficiency (congenital methemoglobinemia with mental retardation, type II) (author's transl)]. , 1981, Annales de medecine interne.

[12]  R. Burgess,et al.  Elution of proteins from sodium dodecyl sulfate-polyacrylamide gels, removal of sodium dodecyl sulfate, and renaturation of enzymatic activity: results with sigma subunit of Escherichia coli RNA polymerase, wheat germ DNA topoisomerase, and other enzymes. , 1980, Analytical biochemistry.

[13]  J. Meldolesi,et al.  Localization and Biosynthesis of NADH-Cytochrome b(5) reductase, an integral membrane protein, in rat liver cells. III. Evidence for the independent insertion and turnover of the enzyme in various subcellular compartments , 1980, The Journal of cell biology.

[14]  J. Meldolesi,et al.  Localization and biosynthesis of NADH-cytochrome b5 reductase, an integral membrane protein, in rat liver cells. II. Evidence that a single enzyme accounts for the activity in its various subcellular locations , 1980, The Journal of cell biology.

[15]  J. Meldolesi,et al.  Localization and biosynthesis of NADH-cytochrome b5 reductase, an integral membrane protein, in rat liver cells. I. Distribution of the enzyme activity in microsomes, mitochondria, and golgi complex , 1980, The Journal of cell biology.

[16]  N. Borgese,et al.  Site of synthesis of rat liver NADH—cytochrome b 5 reductase, an integral membrane protein , 1980, FEBS letters.

[17]  C. Merril,et al.  A highly sensitive silver stain for detecting proteins and peptides in polyacrylamide gels. , 1979, Analytical biochemistry.

[18]  P. Daddona,et al.  Radioimmunochemical quantitation of human adenosine deaminase. , 1979, The Journal of clinical investigation.

[19]  H. Towbin,et al.  Electrophoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets: procedure and some applications. , 1979, Proceedings of the National Academy of Sciences of the United States of America.

[20]  A. De Flora,et al.  Biochemical mechanisms of glucose-6-phosphate dehydrogenase deficiency. , 1978, Proceedings of the National Academy of Sciences of the United States of America.

[21]  E. Beutler,et al.  The removal of leukocytes and platelets from whole blood. , 1976, The Journal of laboratory and clinical medicine.

[22]  S. Takesue,et al.  Immunological similarity between NADH-cytochrome b5 reductase of erythrocytes and liver microsomes. , 1976, Biochimica et biophysica acta.

[23]  B. Masters,et al.  Studies on methemoglobin reductase. Immunochemical similarity of soluble methemoglobin reductase and cytochrome b5 of human erythrocytes with NADH-cytochrome b5 reductase and cytochrome b5 of rat liver microsomes. , 1976, Archives of biochemistry and biophysics.

[24]  C. Junien,et al.  Generalised deficiency of cytochrome b5 reductase in congenital methaemoglobinaemia with mental retardation , 1975, Nature.

[25]  D. Hultquist,et al.  Soluble cytochrome b 5 reductase from human erythrocytes. , 1972, Biochimica et biophysica acta.

[26]  Jeffrey M. Schwartz,et al.  Unstable variant of NADH methemoglobin reductase in Puerto Ricans with hereditary methemoglobinemia. , 1972, The Journal of clinical investigation.

[27]  H. Nakajima,et al.  Studies on methemoglobin reductase. I. Comparative studies of diaphorases from normal and methemoglobinemic erythrocytes. , 1972, The Journal of biological chemistry.

[28]  D E Hultquist,et al.  Catalysis of methaemoglobin reduction by erythrocyte cytochrome B5 and cytochrome B5 reductase. , 1971, Nature: New biology.

[29]  M. Avron,et al.  New method for determining ferrihemoglobin reductase (NADH-methemoglobin reductase) in erythrocytes. , 1968, The Journal of laboratory and clinical medicine.

[30]  L. Ernster,et al.  AN ELECTRON-TRANSPORT SYSTEM ASSOCIATED WITH THE OUTER MEMBRANE OF LIVER MITOCHONDRIA , 1967, The Journal of cell biology.

[31]  E. Scott The relation of diaphorase of human erythrocytes to inheritance of methemoglobinemia. , 1960, The Journal of clinical investigation.

[32]  O. H. Lowry,et al.  Protein measurement with the Folin phenol reagent. , 1951, The Journal of biological chemistry.

[33]  A. Leroux Membrane-bound Cytochrome b 5 Reductase ( Methemoglobin Reductase ) in Human Erythrocytes , 2022 .

[34]  G. Lenoir,et al.  NADH-Cytochrome b 5 Reductase Activity in Lymphoid Cell Lines EXPRESSION OF THE DEFECT IN EPSTEIN-BARR VIRUS TRANSFORMED LYMPHOBLASTOID CELL LINES FROM PATIENTS WITH RECESSIVECONGENITAL METHEMOGLOBINEMIA , 2022 .