The Oxidative Inactivation of Sarcoplasmic Reticulum Ca²⁺-ATPase by Peroxynitrite

References

• Oxygen Free Radicals, M. Tarr, F. Samson. Birkhäuser, Boston 1993
   Google Scholar
• Grisham M. B. Reactive Metabolites of Oxygen and Nitrogen in Biology and Medicine. R.G. Landes Co., Austin 1992
   Google Scholar
• Kukreja R. C., Hess M. L. Free Radicals, Cardio vascular Dysfunction and Protection Strategies. R.G. Landes Co., Austin 1994
   Google Scholar
• Chanock S. J., El Benna J., Smith R. M., Babior B. M. The respiratory burst oxidase. Journal of Biological Chemistry 1994; 269: 24519–24522
   PubMed Web of Science ®Google Scholar
• Koppenol W. H., Moreno J. J., Pryor W. A., Ischiropoulos H., Beckman J. S. Peroxynitrite, a cloked oxidant formed by nitric oxide and superoxide. Chemical Research in Toxicology 1992; 5: 834–842
   PubMed Web of Science ®Google Scholar
• Radi R., Beckman J. S., Bush K. M., Freeman B. A. Peroxynitrite-induced membrane lipid peroxidation: The cytotoxic potential of superoxide and nitric oxide. Archives of Biochemistry and Biophysics 1991; 288: 481–487
   PubMed Web of Science ®Google Scholar
• Ischiropoulos H., Zhu L., Chen J., Tsai M., Martin J. C., Smith C. D., Beckman J. S. Peroxynitrite-mediated tyrosine nitration catalyzed by superoxide dismutase. Archives of Biochemistry and Biophysics 1992; 298: 431–437
   PubMed Web of Science ®Google Scholar
• Beckman J. S., Ischiropoulos H., Zhu L., van der Woerd M., Smith C. D., Chen J., Harrison J., Martin C. D., Tsai M. Kinetics of superoxide dismutase- and ironcatalyzed nitration of phenolics by peroxynitrite. Archives of Biochemistry and Biophysics 1992; 298: 438–445
   PubMed Web of Science ®Google Scholar
• Ischiropoulos H., Zhu L., Beckman J. S. Peroxy nitrite formation from macrophage-derived nitric oxide. Archives of Biochemistry and Biophysics 1992; 298: 446–451
   PubMed Web of Science ®Google Scholar
• Zhu L., Gunn C., Beckman J. S. Bactericidal activity of peroxynitrite. Archives of Biochemistry and Biophysics 1992; 298: 452–457
   PubMed Web of Science ®Google Scholar
• Bauer M. L., Beckman J. S., Bridges R. J., Fuller C. M., Sadis M. Peroxynitrite inhibits sodium uptake in ratcolonic membrane vesicles. Biochimica et Biophysica Acta 1992; 1104: 87–94
   PubMedGoogle Scholar
• Hogg N., Darley-Usmar V. M., Wilson M. T., Moncada S. Production of hydroxyl radicals from the simultaneous generation of superoxide and nitric oxide. Biochemical Journal 1992; 281: 424–919
   Google Scholar
• Stamler J. S., Singel D. J., Loscalzo J. Biochemistry of nitric oxide and its redox-activated forms. Science 1992; 258: 1898–1902
   PubMed Web of Science ®Google Scholar
• Denicola A., Rubbo H., Rodriguez D., Radi R. Peroxynitrite-mediated cytotoxicity to c. Archives of Biochemistry and Biophysics 1993; 304: 279–286
   PubMed Web of Science ®Google Scholar
• Radi R., Rodriguez M., Castro L., Telleri R. Inhibition of mitochondrialelectron transport by peroxynitrite. Archives of Biochemistry and Biophysics 1994; 308: 89–95
   PubMed Web of Science ®Google Scholar
• Rubbo H., Denicola A., Radi R. Peroxynitrite inactivates thiol-containing enzymes of trypanosomacruzi energetic metabolism and inhibits cell respiration. Archives of Biochemistry and Biophysics 1994; 308: 96–102
   PubMed Web of Science ®Google Scholar
• Augusto O., Gatti R. M., Radi R. Spin-trapping studies of peroxynitrite decomposition and of 3-morpholinosydnonimine N-ethylcarbamide auto-oxidation: Direct evidence for metal-independent formation of free radical intermediates. Archives of Biochemistry and Biophysics 1994; 310: 118–125
   PubMed Web of Science ®Google Scholar
• Huie R. E., Padmaja S. Reaction of NO with O2−. Free Radical Research Communications 1993; 18: 195–199
   PubMed Web of Science ®Google Scholar
• Murphy M. E., Sies H. Reversible conversion of nitroxyl anion to nitric oxide by superoxide dismutase. Proceedings of the National Academy of Sciences of the USA 1991; 88: 10860–10864
   PubMed Web of Science ®Google Scholar
• Crow J. P., Spruell C., Chen J., Gunn C., Ischiropoulos H., Tsai M., Smith C. D., Radi R., Koppenol W. H., Beckman J. S. On the pH-dependent yield of hydroxyl radical products from peroxynitrite. Free Radical Biology and Medicine 1994; 16: 331–338
   PubMed Web of Science ®Google Scholar
• van der Vliet A., O'Neill C., Halliwell B., Cross C. E., Kaur H. Aromatic hydroxylation and nitration of phenylalanine and tyrosineby peroxynitrite. FEBS Letters 1994; 339: 89–92
   PubMed Web of Science ®Google Scholar
• Radi R., Beckman J. S., Bush K. M., Freeman B. A. Peroxynitrite oxidation of sulfhydry ls. Journal of Biological Chemistry 1991; 266: 4244–4250
   PubMed Web of Science ®Google Scholar
• Moreno J. J., Pryor W. A. Inactivation of α-1-proteinase inhibitor by peroxynitrite. Chemical Research in Toxicology 1992; 5: 425–431
   PubMed Web of Science ®Google Scholar
• Pryor W. A., Jin X., Squadrito G. L. One- and two-electron oxidations of methionine by peroxynitrite. Proceedings of the National Academy of Sciences USA 1994; 91: 11173–11177
   PubMed Web of Science ®Google Scholar
• Shi X., Lenhart A., Mao Y. ESR-spin trapping investigation on peroxynitrite decomposition: No evidence for hydroxyl radical production. Biochemical and Biophysical Research Communications 1994; 203: 1515–1521
   PubMed Web of Science ®Google Scholar
• Bartlett D., Church D. F., Bounds P. L., Koppenol W. H. The kinetics of the oxidation of L-ascorbic acid by peroxynitrite. Free Radical Biology and Medicine 1995; 18: 85–92
   PubMed Web of Science ®Google Scholar
• Beckman J. S., Beckman T. W., Chen J., Marshall P. A., Freeman B. A. Apparent hydroxyl radical production by peroxynitrite: Implications for endothelial injury from nitric oxide and superoxide. Proceedings of the National Academy of Sciences of the USA 1990; 87: 1620–1624
   PubMed Web of Science ®Google Scholar
• Radi R., Cosgrove T. P., Beckman J. S., Freeman B. A. Peroxynitrite-induced luminol cheniilumines-cence. Biochemical Journal 1993; 290: 51–57
   PubMed Web of Science ®Google Scholar
• Kooy N. W., Royall J. A. Agonist-induced peroxynitrite production from endothelial cells. Archives of Biochemistry and Biophysics 1994; 310: 352–359
   PubMed Web of Science ®Google Scholar
• Nicotera P., Kass G. E.N., Duddy S. K., Orrenius S. Calcium and signal transudation in oxidative cell damage. Calcium, Oxygen Radicals and Cellular Damage, C. J. Duncan. Cambridge University Press. 1991; 17–33
   Google Scholar
• Chaudiere J. Some chemical and biochemical constraints of oxidative stress in living cells. Free Radical Damage and its Control, C. A. Rice-Evans, R. H. Burdon. Elsevier, New York 1994; 25–66
   Google Scholar
• Kukreja R. C., Okabe E., Schrier G. M., Hess M. L. Oxygen radical-mediated lipid peroxidation and inhibition of Ca 2+-ATPase activity of cardiac sarcoplasmic reticulum. Archives of Biochemistry and Biophysics 1988; 261: 447–457
   PubMed Web of Science ®Google Scholar
• Kukreja R. C., Hess M. L. The oxygen free radical system: From equations through membrane-protein interactions to cardiovascular injury and protection. Cardiovascular Research 1992; 26: 641–655
   PubMed Web of Science ®Google Scholar
• Scherer N. M., Deamer D. W. Oxidative stress impairs the function of sarcoplasmic reticulum by oxidation of sulhydryl groups in the Ca2+-ATPase. Archives of Biochemistry and Biophysics 1986; 246: 589–601
   PubMed Web of Science ®Google Scholar
• Nakane M., Schmidt H. H.W., Pollock J. S., Förstermann U., Murad F. Cloned human brain nitric oxide synthase is highly expressed in skeletal muscle. FEBS. Letters 1993; 316: 175–180
   Google Scholar
• Kobzik L., Reid M. B., Bredt D. S., Stamler J. S. Nitric oxide in skeletal muscle. Nature 1994; 372: 546–548
   PubMed Web of Science ®Google Scholar
• Pryor W. A., Cueto R., Jin X., Koppenol W. H., Ngu-Schwemlein M., Squadrito G. L., Uppu P. L., Uppu R. M. A practical method for preparing peroxynitrite solutions of low ionic strength and free of hydrogen peroxide. Free Radical Biology and Medicine 1995; 18: 75–83
   PubMed Web of Science ®Google Scholar
• Hughes M. N., Nicklin H. G. The chemistry of pernitrites. Part I. Kinetics of decomposition of pernitrous acid. Journal of the Chemical Society (A) 1968; 450–452
   Google Scholar
• Saito A., Seiler S., Chu A., Fleischer S. Preparation and morphology of sarcoplasmic reticulum terminal cisternae from rabbit skeletal muscle. Journal of Cell Biology 1984; 99: 875–885
   PubMed Web of Science ®Google Scholar
• Lanzetta P. A., Alvarez L. J., Reinach P. S., Candia O. A. An important assay for nanomole amounts of inorganic phosphate. Analytical Biochemistry 1979; 100: 95–97
   PubMed Web of Science ®Google Scholar
• Giulivi C., Davies K. J.A. Dityrosine: A marker for oxidatively modified proteins and selective proteolysis. Methods in Enzymology 1994; 233: 363–371
   PubMed Web of Science ®Google Scholar
• Guptasarma P., Balasubramanian D., Matsugo S., Saito I. Hydroxyl radical mediated damage to proteins, with special reference to the crystallins. Biochemistry 1992; 31: 4296–4303
   PubMed Web of Science ®Google Scholar
• Lakowicz J. R. Principles of Fluorescence Spectroscopy. Plenum Press, New York 1983; 1: 260
   Google Scholar
• Ellman G. L. Tissue sulfhydryl groups. Archives of Biochemistry and Biophysics 1959; 82: 47–70
   Web of Science ®Google Scholar
• Murphy A. J. Sulfhydryl group modification of sarcoplasmic reticulum membranes. Biochemistry 1976; 15: 4492–4496
   PubMedGoogle Scholar
• Brown W. D. Reduction of protein disulfide bonds by sodium borohydride. Biochimica et Biophysica Acta 1960; 44: 365–367
   Google Scholar
• Levine R. L., Williams J. A., Stadtman E. R., Shacter E. Carbonyl assays for determination of oxidatively modified proteins. Methods in Enzymology 1994; 233: 346–363
   PubMed Web of Science ®Google Scholar
• Barrabin H., Scofano H. M., Inesi G. Adeno-sinetriphosphatase site stoichiometry in sarcoplasmic reticulum vesicles and purified enzyme. Biochemistry 1982; 23: 1542–1548
   Google Scholar
• Coll R. J., Murphy A. J. Purification of the CaATPase of sarcoplasmic reticulum by affinity chromatography. Journal of Biological Chemistry 1984; 259: 14249–14254
   PubMedGoogle Scholar
• Lowry O. H., Rosebrough N. J., Farr A. L., Randall R. J. Protein measurement with the folin phenol reagent. Journal of Biological Chemistry 1951; 193: 265–275
   PubMed Web of Science ®Google Scholar
• Cordis G. A., Maulik N., Bagchi D., Engelman R. M., Das D. K. Estimation of the extent of lipid peroxida-tion in the ischemic and reperfused heart by monitoring lipid metabolic products with the aid of high-performance liquid chromatography. Journal of Chromatography 1993; 632: 97–103
   PubMedGoogle Scholar
• Laemmli U. K. Cleavage of structural proteins during the assembly of the head of bacteriophage T4. Nature 1970; 227: 680–685
   PubMed Web of Science ®Google Scholar
• Towbin H., Staehelin T., Gordon J. Electro-phoretic transfer of proteins from polyacrylamide gels to nitrocellulose sheets. Procedure and some applications. Proceedings of the National Academy of Sciences of the USA 1979; 76: 4350–4354
   PubMed Web of Science ®Google Scholar
• Yao Y., Schöneich Ch., Squier T. C. Resolution of structural changes associated with calcium activation of calmodulin using frequency domaine fluorescence spectroscopy. Biochemistry 1994; 33: 7797–7810
   PubMed Web of Science ®Google Scholar
• Brandl C. J., Green N. M., Korczak B., MacLennan DH. Two Ca-ATPase genes: Homologies and mechanis tic implications of deduced amino acid sequences. Cell 1986; 44: 597–607
   PubMedGoogle Scholar
• Stadtman E. R. Oxidation of free amino acids and amino acid residues in proteins by radiolysis and by metal-catalyzed reactions. Annual Reviews in Biochemistry 1993; 62: 797–821
   PubMed Web of Science ®Google Scholar
• Neuzil J., Gebicki J. M., Stocker R. Radical-induced chain oxidation of proteins and its inhibition by chain-breaking antioxidants. Biochemical Journal 1993; 293: 601–606
   PubMed Web of Science ®Google Scholar
• Grierson L., Hildenbrand K., Bothe E. Intra molecular transformation reaction of the glutathione thiyl radical into a non-sulphur-centred radical: A pulse radiolysis and EPR study. International Journal of Radiation Biology 1992; 62: 265–277
   PubMed Web of Science ®Google Scholar
• Arkhipenko Y.V., Kagan V. E., Kozlov Y.P. Mod ification of the enzyme system of Ca2+ transport in the sarcoplasmic reticulum in lipid peroxidation. Molecular mechanisms underlying the alteration of Ca-ATPase activity. Biokhimiya (Moscow) 1983; 48: 376–383
   Google Scholar
• Sevilla M. D., Mengyao Y., Becker D. Thiol peroxyl radical formation from the reaction of cysteine thiyl radical with molecular oxygen: An ESR investigation. Biochemical and Biophysical Research Communications 1988; 155: 405–410
   PubMed Web of Science ®Google Scholar
• Zhang X., Zhang N., Schuchmann H.-P., von Sonntag C. Pulse radiolysis of 2-mercaptoethanol in oxygenated aqueous solution. Generation and reactions of thiylperoxyl radical. Journal of Physical Chemistry 1994; 98: 6541–6547
   Web of Science ®Google Scholar
• Göbl M., Bonifa'ić M., Asmus K.-D. Substituent effects on the stability of three-electron-bonded radicals and radical ions from organic sulfur compounds. Journal of the American Chemical Society 1984; 106: 5984–5988
   Web of Science ®Google Scholar
• Akhlaq M. S., von Sonntag C. Intermolecular H-abstraction of thiyl radicals from thiols and the intra molecular complexing of the thiyl radical with the thiol group in 1,4-dithiothreitol. A pulse radiolysis study. Zeitschrift für Naturforschung 1986; 42c: 134–140
   Google Scholar
• Willson R. L. Pulse radiolysis studies of electron transfer in aqueous disulfide solutions. Chemical Communications 1970; 1425–1426
   Google Scholar
• Redpath J. L. Pulse radiolysis of dithiothreitol. Radiation Research 1973; 54: 364–374
   PubMed Web of Science ®Google Scholar
• Candeias L. P., Patel K. B., Stratford M. R.L., Wardman P. Free hydroxyl radicals are formed on reaction between the neutrophil-derived species super-oxide anion and hypochlorous acid. FEBS Letters 1993; 333: 151–153
   PubMed Web of Science ®Google Scholar
• Pryor W. A., Squadrito G. L. The chemistry of peroxynitrite: a product from the reaction of nitric oxide with superoxide. American Journal of Physiology 1995; 268(Lung Cell. Mol. Physiol. 12)L699–L722
   PubMedGoogle Scholar