The DOI matches its Crossref record; 147 of the 147 references it cites were found in a registry or an index.
Peroxynitrite reactivity with amino acids and proteins
Abstract
Peroxynitrite, the product of the fast reaction between nitric oxide ((*)NO) and superoxide O(2)(*-) radicals, is an oxidizing and nitrating agent which is able to traverse biological membranes. The reaction of peroxynitrite with proteins occurs through three possible pathways. First, peroxynitrite reacts directly with cysteine, methionine and tryptophan residues. Second, peroxynitrite reacts fast with transition metal centers and selenium-containing amino acids. Third, secondary free radicals arising from peroxynitrite homolysis such as hydroxyl and nitrogen dioxide, and the carbonate radical formed in the presence of carbon dioxide, react with protein moieties too. Nitration of tyrosine residues is being recognized as a marker of the contribution of nitric oxide to oxidative damage. Peroxynitrite-dependent tyrosine nitration is likely to occur through the initial reaction of peroxynitrite with carbon dioxide or metal centers leading to secondary nitrating species. The preferential protein targets of peroxynitrite and the role of proteins in peroxynitrite detoxifying pathways are discussed.
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Interestingly, the nitroproteome appears to be quite specific, and pathological responses may be due to modification of particularly sensitive proteins, including those that regulate signaling and cell metabolism (49–52).”
From What Part of NO Don't You Understand? Some Answers to the Cardinal Questions in Nitric Oxide Biology (2010) · cites this paper as [49]
In the citing paper
“Interestingly, the nitroproteome appears to be quite specific, and pathological responses may be due to modification of particularly sensitive proteins, including those that regulate signaling and cell metabolism (49–52).”
From What Part of NO Don't You Understand? Some Answers to the Cardinal Questions in Nitric Oxide Biology (2010) · cites this paper as [49]
In the citing paper
“The protonated form of ONOO— (ONOOH, pKa = 6.5 to 6.8) decomposes rapidly to RNS, yielding approximately 28% of free •NO2 and •OH radical [123], Figure 5 down.”
From The Role of Reactive Species on Innate Immunity (2022) · cites this paper as [123]
In the citing paper
“Peroxynitrite and reactive species derived from it (e.g., nitrogen dioxide) are important in inflammatory responses [85] and can modulate cell signaling [87-90], in part by promoting the oxidation or nitration of a broad range of biomolecules [62].”
From Regulation of obesity and insulin resistance by nitric oxide (2014) · cites this paper as [87]
Citations
Cites
Beckman, J. S., Beckman, T. W., Chen, J., Marshall, P. A., & Freeman, B. A. (1990) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.87.4.1620 · Cited by 7,029
Peroxynitrite oxidation of sulfhydryls.
Radí, R., Beckman, J. S., Bush, K., & Freeman, B. Α. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)64313-7 · Cited by 2,492
The reaction of NO with superoxide
Huie, R. E., & Padmaja, S. (1993) · Free Radical Research Communications · doi:10.3109/10715769309145868 · Cited by 2,121
Peroxynitrite-mediated tyrosine nitration catalyzed by superoxide dismutase
Ischiropoulos, H., Zhu, L., Chen, J., Tsai, M., Martin, J. C., Smith, C. D. L., & Beckman, J. S. (1992) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(92)90431-u · Cited by 1,499
Formation of nitric oxide-derived inflammatory oxidants by myeloperoxidase in neutrophils
Eiserich, J. P., Hristova, M., Cross, C. E., Jones, A. D., Freeman, B. A., Halliwell, B., & van der Vliet, A. (1998) · Nature · doi:10.1038/34923 · Cited by 1,496
Peroxynitrite, a cloaked oxidant formed by nitric oxide and superoxide
Koppenol, W. H., Moreno, J. J., Pryor, W. A., Ischiropoulos, H., & Beckman, J. S. (1992) · Chemical Research in Toxicology · doi:10.1021/tx00030a017 · Cited by 1,338
Formation of reactive nitrogen species during peroxidase-catalyzed oxidation of nitrite
van der Vliet, A., Eiserich, J. P., Halliwell, B., & Cross, C. E. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.12.7617 · Cited by 780
MacMillan-Crow, L.-A., Crow, J. P., Kerby, J. D., Beckman, J. S., & Thompson, J. A. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.21.11853 · Cited by 769
Unraveling peroxynitrite formation in biological systems
Radi, R., Peluffo, G., Alvarez, M. N., Naviliat, M., & Cayota, A. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00373-7 · Cited by 735
Inhibition of Mitochondrial Electron Transport by Peroxynitrite
Radi, R., Rodriguez, M., Castro, L., & Telleri, R. (1994) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1994.1013 · Cited by 693
Peroxynitrite reductase activity of bacterial peroxiredoxins
Bryk, R., Griffin, P. R., & Nathan, C. (2000) · Nature · doi:10.1038/35025109 · Cited by 679
Kissner, R., Nauser, T., Bugnon, P., Lye, P. G., & Koppenol, W. H. (1997) · Chemical Research in Toxicology · doi:10.1021/tx970160x · Cited by 629
Denicola, A., Freeman, B. A., Trujillo, M., & Radi, R. (1996) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1996.0363 · Cited by 593
Aconitase is readily inactivated by peroxynitrite, but not by its precursor, nitric oxide.
Castro, L., Rodriguez, M., & Radi, R. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)43894-x · Cited by 589
Superoxide and peroxynitrite inactivate aconitases, but nitric oxide does not.
Hausladen, A., & Fridovich, I. (1994) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(18)43893-8 · Cited by 585
Nitrogen dioxide and carbonate radical anion: two emerging radicals in biology
Augusto, O., Bonini, M. G., Amanso, A. M., Linares, E., Santos, C. C. X., & De Menezes, S. L. (2002) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(02)00786-4 · Cited by 555
Greenacre, S., & Ischiropoulos, H. (2001) · Free Radical Research · doi:10.1080/10715760100300471 · Cited by 500
Glutathione Peroxidase Protects against Peroxynitrite-mediated Oxidations
Sies, H., Sharov, V. S., Klotz, L., & Briviba, K. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.44.27812 · Cited by 488
Brennan, M.-L., Wu, W., Fu, X., Shen, Z., Song, W., Frost, H., Vadseth, C., Narine, L., Lenkiewicz, E., Borchers, M. T., et al. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m112400200 · Cited by 486
Okamoto, T., Akaike, T., Sawa, T., Miyamoto, Y., van der Vliet, A., & Maeda, H. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m102417200 · Cited by 468
Effects of peroxynitrite‐induced protein modifications on tyrosine phosphorylation and degradation
Gow, A. J., Duran, D., Malcolm, S., & Ischiropoulos, H. (1996) · FEBS Letters · doi:10.1016/0014-5793(96)00347-x · Cited by 449
Landino, L. M., Crews, B. C., Timmons, M. D., Morrow, J. D., & Marnett, L. J. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.26.15069 · Cited by 423
Ara, J. E., Przedborski, S., Naini, A., Jackson-Lewis, V. R., Trifiletti, R. R., Horwitz, J., & Ischiropoulos, H. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.13.7659 · Cited by 414
Diffusion of peroxynitrite across erythrocyte membranes
Denicola, A., Souza, J. M., & Radi, R. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.7.3566 · Cited by 403
Metabolic Enzymes of Mycobacteria Linked to Antioxidant Defense by a Thioredoxin-Like Protein
Bryk, R., Lima, C. D., Erdjument‐Bromage, H., Tempst, P., & Nathan, C. (2002) · Science · doi:10.1126/science.1067798 · Cited by 400
Aromatic hydroxylation and nitration of phenylalanine and tyrosine by peroxynitrite
van der Vliet, A., O’neill, C. A., Halliwell, B. B., Cross, C. E., & Kaur, H. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)80391-9 · Cited by 381
Tyrosine Modification by Reactive Nitrogen Species: A Closer Look
Vandervliet, A., Eiserich, J. P., O’Neill, C., Halliwell, B. B., & Cross, C. E. (1995) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1995.1303 · Cited by 373
Proteomic method identifies proteins nitrated in vivo during inflammatory challenge
Aulak, K. S., Miyagi, M., Yan, L., West, K. A., Massillon, D., Crabb, J. W., & Stuehr, D. J. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.221269198 · Cited by 350
Prütz, W. A., Mönig, H., Butler, J., & Land, E. J. (1985) · Archives of Biochemistry and Biophysics · doi:10.1016/0003-9861(85)90780-5 · Cited by 338
Kong, S. K., Yim, M. B., Stadtman, E. R., & Chock, P. B. (1996) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.93.8.3377 · Cited by 337
Metabolic Fate of Peroxynitrite in Aqueous Solution
Pfeiffer, S., Gorren, A. C. F., Schmidt, K., Werner, E. R., Hansert, B., Bohle, D. S., & Mayer, B. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.6.3465 · Cited by 329
One- and two-electron oxidations of methionine by peroxynitrite.
PRYOR, W. A., Jin, X., & Squadrito, G. L. (1994) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.91.23.11173 · Cited by 324
Factors Determining the Selectivity of Protein Tyrosine Nitration
Souza, J. M., Daikhin, E., Yudkoff, M., Raman, C. S., & Ischiropoulos, H. (1999) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1999.1480 · Cited by 315
Sulfenic Acid Formation in Human Serum Albumin by Hydrogen Peroxide and Peroxynitrite
Carballal, S., Radí, R., KIRK, M. C., Barnes, S., Freeman, B. Α., & Álvarez, B. (2003) · Biochemistry · doi:10.1021/bi027434m · Cited by 312
Electron transfer reaction rates and equilibria of the carbonate and sulfate radical anions
Huie, R. E., Clifton, C. L., & Neta, P. (1991) · International Journal of Radiation Applications and Instrumentation Part C Radiation Physics and Chemistry · doi:10.1016/1359-0197(91)90065-a · Cited by 312
Protection against peroxynitrite
Arteel, G. E., Briviba, K., & Sies, H. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)00073-3 · Cited by 305
Direct EPR Detection of the Carbonate Radical Anion Produced from Peroxynitrite and Carbon Dioxide
Bonini, M. G., Radi, R., Ferrer-Sueta, G., Ferreira, A. M. D. C., & Augusto, O. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.16.10802 · Cited by 293
Zou, M., Martin, C., & Ullrich, V. (1997) · Biological Chemistry · doi:10.1515/bchm.1997.378.7.707 · Cited by 289
Galdo, N. A. R., Clementi, E., Melani, M., Boveris, A., Cadenas, E., Moncada, S., & Poderoso, J. J. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3590139 · Cited by 278
Santos, C. X. C., Anjos, E. I., & Augusto, O. (1999) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1999.1491 · Cited by 275
An activity in rat tissues that modifies nitrotyrosine-containing proteins
Kamisaki, Y., Wada, K., Bian, K., Balabanlı, B., Davis, K. L., Martin, E., Behbod, F., Lee, Y.-C., & Murad, F. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.20.11584 · Cited by 275
Pathways of peroxynitrite oxidation of thiol groups
Quijano, C., Álvarez, B., Gatti, R. M., Augusto, O., & Radí, R. (1997) · Biochemical Journal · doi:10.1042/bj3220167 · Cited by 261
Proteolytic Degradation of Tyrosine Nitrated Proteins
Souza, J. M., Choi, I. Y., Chen, Q., Weisse, M., Daikhin, E., Yudkoff, M., Obin, M. S., Ara, J. E., Horwitz, J., & Ischiropoulos, H. (2000) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2000.1940 · Cited by 260
Peroxynitrite-Dependent Tryptophan Nitration
Álvarez, B., Rubbo, H., KIRK, M. C., Barnes, S., Freeman, B. Α., & Radí, R. (1996) · Chemical Research in Toxicology · doi:10.1021/tx950133b · Cited by 259
Hydroxyl Radical Formation during Peroxynitrous Acid Decomposition
Coddington, J. W., Hurst, J. K., & Lymar, S. V. (1999) · Journal of the American Chemical Society · doi:10.1021/ja982887t · Cited by 257
Kinetics of Peroxynitrite Reaction with Amino Acids and Human Serum Albumin
Álvarez, B., Ferrer‐Sueta, G., Freeman, B. Α., & Radí, R. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.2.842 · Cited by 253
Inactivation of .alpha.1-proteinase inhibitor by peroxynitrite
Moreno, J. J., & Pryor, W. A. (1992) · Chemical Research in Toxicology · doi:10.1021/tx00027a017 · Cited by 250
Crow, J. P., Beckman, J. S., & McCord, J. M. (1995) · Biochemistry · doi:10.1021/bi00011a008 · Cited by 244
Interaction of myeloperoxidase with peroxynitrite
Floris, R., Piersma, S. R., Guang, Y. A. N. G., Jones, P. M., & Wever, R. (1993) · European Journal of Biochemistry · doi:10.1111/j.1432-1033.1993.tb18091.x · Cited by 237
Zou, M., & Ullrich, V. (1996) · FEBS Letters · doi:10.1016/0014-5793(96)00160-3 · Cited by 231
John, G. S., Brot, N., Ruan, J., Erdjument‐Bromage, H., Tempst, P., Weissbach, H., & Nathan, C. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.161295398 · Cited by 206
Takakura, K., Beckman, J. S., MacMillan-Crow, L. A., & Crow, J. P. (1999) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1999.1374 · Cited by 203
Bonini, M. G., & Augusto, O. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m008456200 · Cited by 192
The kinetics of the oxidation of l-ascorbic acid by peroxynitrite
Bartlett, D., Church, D. F., Bounds, P. L., & Koppenol, W. H. (1995) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(94)e0133-4 · Cited by 192
Stachowiak, O., Dolder, M., Wallimann, T., & Richter, C. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.27.16694 · Cited by 189
Thomson, L., Trujillo, M., Telleri, R., & Radi, R. (1995) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1995.1321 · Cited by 186
Reaction of Peroxynitrite with Mn-Superoxide Dismutase
Quijano, C., Hernández-Saavedra, D., Castro, L., McCord, J. M., Freeman, B. Α., & Radí, R. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m009429200 · Cited by 186
Peroxynitrite Decomposition Catalysts
Stern, M. K., Jensen, M. P., & Kramer, K. S. (1996) · Journal of the American Chemical Society · doi:10.1021/ja961279f · Cited by 184
Glyceraldehyde-3-Phosphate Dehydrogenase Inactivation by Peroxynitrite
Souza, J. M., & Radí, R. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1998.0932 · Cited by 179
Trujillo, M., & Radí, R. (2002) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2619 · Cited by 179
Interaction of Nitrous Acid with Hydrogen Peroxide and with Water
Anbar, M., & Taube, H. (1954) · Journal of the American Chemical Society · doi:10.1021/ja01653a007 · Cited by 179
Tyrosine Nitration by Simultaneous Generation of ⋅NO and O⨪2 under Physiological Conditions
Goldstein, S., Czapski, G., Lind, J., & Merényi, G. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.5.3031 · Cited by 177
Wong, C., Zhou, Y., Ng, R. W. M., Kung, H., & Jin, D. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m106846200 · Cited by 174
Nitration and Inactivation of Tyrosine Hydroxylase by Peroxynitrite
Blanchard-Fillion, B., Souza, J. M., Friel, T., Jiang, G. C. ‐., Vrana, K. E., Sharov, V. S., Barrón, L., Schöneich, C., Quijano, C., Álvarez, B., et al. (2001) · Journal of Biological Chemistry · doi:10.1074/jbc.m105564200 · Cited by 172
The Reaction of Ebselen with Peroxynitrite
Masumoto, H., & Sies, H. (1996) · Chemical Research in Toxicology · doi:10.1021/tx950115u · Cited by 171
Augusto, O., Gatti, R. M., & Radí, R. (1994) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1994.1147 · Cited by 170
Gunther, M. R., Hsi, L. C., Curtis, J. F., Gierse, J. K., Marnett, L. J., Eling, T. E., & Mason, R. P. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.27.17086 · Cited by 169
Peroxynitrite modulates tyrosine‐dependent signal transduction pathway of human erythrocyte band 3
Mallozzi, C., Stasi, A. M. M. D., & Minetti, M. (1997) · The FASEB Journal · doi:10.1096/fasebj.11.14.9409547 · Cited by 166
The Oxidative Inactivation of Sarcoplasmic Reticulum Ca2+-ATPase by Peroxynitrite
Viner, R. I., Hühmer, A. F. R., Bigelow, D. J., & Schöneich, C. (1996) · Free Radical Research · doi:10.3109/10715769609088022 · Cited by 161
Nitration and Hydroxylation of Phenolic Compounds by Peroxynitrite
Ramezanian, M. S., Padmaja, S., & Koppenol, W. H. (1996) · Chemical Research in Toxicology · doi:10.1021/tx950135w · Cited by 157
Ferrer‐Sueta, G., Batinic̈‐Haberle, I., Spasojević, I., Fridovich, I., & Radí, R. (1999) · Chemical Research in Toxicology · doi:10.1021/tx980245d · Cited by 157
The effect of oxygen, antioxidants, and superoxide radical on tyrosine phenoxyl radical dimerization
Hunter, E. P. L., Desrosiers, M. F., & Simic, M. G. (1989) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(89)90064-6 · Cited by 153
Arteel, G. E., Mostert, V., Oubrahim, H., Briviba, K., Abel, J., & Sies, H. (1998) · PubMed · Cited by 152
Rapid and irreversible inhibition of creatine kinase by peroxynitrite
Konorev, E. A., Hogg, N., & Kalyanaraman, B. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00413-x · Cited by 152
Master, S. S., Springer, B., Sander, P., Boettger, E. C., Deretic, V. P., & Timmins, G. S. (2002) · Microbiology · doi:10.1099/00221287-148-10-3139 · Cited by 151
Berlett, B. S., Levine, R. L., & Stadtman, E. R. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.6.2784 · Cited by 151
Interaction of peroxynitrite with selenoproteins and glutathione peroxidase mimics
Sies, H., & Arteel, G. E. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00253-7 · Cited by 149
Peroxynitrite‐mediated oxidation of albumin to the protein‐thiyl free radical
Gatti, R. M., Radí, R., & Augusto, O. (1994) · FEBS Letters · doi:10.1016/0014-5793(94)00625-3 · Cited by 146
Balazy, M., Kaminski, P. M., Mao, K., Tan, J., & Wolin, M. S. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.48.32009 · Cited by 143
CO2-Catalyzed One-Electron Oxidations by Peroxynitrite: Properties of the Reactive Intermediate
Lymar, S. V., & Hurst, J. K. (1998) · Inorganic Chemistry · doi:10.1021/ic970946i · Cited by 141
Regulation of xanthine oxidase by nitric oxide and peroxynitrite
Lee, C.-I., Liu, X., & Zweier, J. L. (2000) · Journal of Biological Chemistry · doi:10.1074/jbc.275.13.9369 · Cited by 140
Inactivation of Glutathione Peroxidase by Peroxynitrite
Padmaja, S., Squadrito, G. L., & Pryor, W. A. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0407 · Cited by 134
Linares, E., Giorgio, S., Mortara, R. A., Santos, C. X. C., Yamada, A. T., & Augusto, O. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00516-0 · Cited by 131
Briviba, K., Roussyn, I., Sharov, V. S., & Sies, H. (1996) · Biochemical Journal · doi:10.1042/bj3190013 · Cited by 130
Schieke, S. M., Briviba, K., Klotz, L., & Sies, H. (1999) · FEBS Letters · doi:10.1016/s0014-5793(99)00372-5 · Cited by 130
Klebl, B., Ayoub, A. T., & Pette, D. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)00053-2 · Cited by 128
Irie, Y., Saeki, M., Kamisaki, Y., Martin, E., & Murad, F. (2003) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1131756100 · Cited by 128
Crystal Structure of the Antioxidant Enzyme Glutathione Reductase Inactivated by Peroxynitrite
Savvides, S. N., Scheiwein, M., Böhme, C. C., Arteel, G. E., Karplus, P. A., Becker, K., & Schirmer, R. H. (2002) · Journal of Biological Chemistry · doi:10.1074/jbc.m108190200 · Cited by 127
Asahi, M., Fujii, J., Takao, T., Kuzuya, T., Hori, M., Shimonishi, Y., & Taniguchi, N. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.31.19152 · Cited by 122
Keyer, K., & Imlay, J. A. (1997) · Journal of Biological Chemistry · doi:10.1074/jbc.272.44.27652 · Cited by 119
Kinetic Study of the Reaction of Glutathione Peroxidase with Peroxynitrite
Briviba, K., Kissner, R., Koppenol, W. H., & Sies, H. (1998) · Chemical Research in Toxicology · doi:10.1021/tx980086y · Cited by 116
The Biological Chemistry of Peroxynitrite
Radí, R., Denicola, A., Álvarez, B., Ferrer‐Sueta, G., & Rubbo, H. (2000) · Elsevier eBooks · doi:10.1016/b978-012370420-7/50005-8 · Cited by 115
Kuhn, D. M., Aretha, C. W., & Geddes, T. J. (1999) · Journal of Neuroscience · doi:10.1523/jneurosci.19-23-10289.1999 · Cited by 115
Diffusion of Peroxynitrite in the Presence of Carbon Dioxide
Romero, N., Denicola, A., Souza, J. M., & Radí, R. (1999) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1999.1272 · Cited by 113
Role of the Carbonate Radical Anion in Tyrosine Nitration and Hydroxylation by Peroxynitrite
Santos, C. X. C., Bonini, M. G., & Augusto, O. (2000) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2000.1751 · Cited by 105
Reactivity of hydroxyl with tyrosine in aqueous solution studied by pulse radiolysis
Solar, S., Solar, W., & Getoff, N. (1984) · The Journal of Physical Chemistry · doi:10.1021/j150654a030 · Cited by 99
Castro, L. A., Robalinho, R. L., Cayota, A., Meneghini, R., & Radi, R. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1998.0898 · Cited by 98
Roberts, E. S., Lin, H.-L., Crowley, J. R., Vuletich, J. L., Osawa, Y., & Hollenberg, P. F. (1998) · Chemical Research in Toxicology · doi:10.1021/tx980099b · Cited by 98
Direct and Indirect Oxidations by Peroxynitrite
Goldstein, S., & Czapski, G. (1995) · Inorganic Chemistry · doi:10.1021/ic00120a006 · Cited by 96
Daiber, A., Herold, S., Schöneich, C., Namgaladze, D., Peterson, J. A., & Ullrich, V. (2000) · European Journal of Biochemistry · doi:10.1046/j.1432-1033.2000.01768.x · Cited by 96
Myoglobin Catalyzes Its Own Nitration
Bourassa, J. L., Ives, E. P., Marqueling, A. L., Shimanovich, R., & Groves, J. T. (2001) · Journal of the American Chemical Society · doi:10.1021/ja015621m · Cited by 95
Koppenol, W. H., & Kissner, R. (1998) · Chemical Research in Toxicology · doi:10.1021/tx970200x · Cited by 93
Requirements for heme and thiols for the nonenzymatic modification of nitrotyrosine
Balabanlı, B., Kamisaki, Y., Martin, E., & Murad, F. (1999) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.96.23.13136 · Cited by 91
Alayash, A. I., Ryan, B. A. B., & Cashon, R. E. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0449 · Cited by 89
Schopfer, F. J., Galdo, N. A. R., Carreras, M. C., Álvarez, B., Radí, R., Boveris, A., Cadenas, E., & Poderoso, J. J. (2000) · Biochemical Journal · doi:10.1042/0264-6021:3490035 · Cited by 86
Reduction of Methionine Selenoxide to Selenomethionine by Glutathione
Assmann, A., Briviba, K., & Sies, H. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0462 · Cited by 79
Nitration of succinyl-CoA:3-oxoacid CoA-transferase in rats after endotoxin administration
Marcondes, S., Turko, I. V., & Murad, F. (2001) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.141222598 · Cited by 78
Function of Thioredoxin Reductase as a Peroxynitrite Reductase Using Selenocystine or Ebselen
Arteel, G. E., Briviba, K., & Sies, H. (1999) · Chemical Research in Toxicology · doi:10.1021/tx980223r · Cited by 77
Zhang, H., Joseph, J., Feix, J. B., Hogg, N., & Kalyanaraman, B. (2001) · Biochemistry · doi:10.1021/bi002958c · Cited by 77
Peroxynitrite Inactivates Tryptophan Hydroxylase via Sulfhydryl Oxidation
Kuhn, D. M., & Geddes, T. J. (1999) · Journal of Biological Chemistry · doi:10.1074/jbc.274.42.29726 · Cited by 75
Sampson, J. B., Rosen, H., & Beckman, J. S. (1996) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(96)69023-5 · Cited by 74
Wong, P., Eiserich, J. P., Reddy, S., López, C. L., Cross, C. E., & van der Vliet, A. (2001) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2001.2532 · Cited by 72
[33] Kinetic analysis of reactivity of peroxynitrite with biomolecules
Radí, R. (1996) · Methods in enzymology on CD-ROM/Methods in enzymology · doi:10.1016/s0076-6879(96)69036-3 · Cited by 69
Yamakura, F., Matsumoto, T., Fujimura, T., Taka, H., Murayama, K., Imai, T., & Uchida, K. (2001) · Biochimica et Biophysica Acta (BBA) - Protein Structure and Molecular Enzymology · doi:10.1016/s0167-4838(01)00212-6 · Cited by 69
Denitration of peroxynitrite-treated proteins by ‘protein nitratases’ from rat brain and heart
Kuo, W., Kanadia, R., Shanbhag, V. P., & Toro, R. (1999) · Molecular and Cellular Biochemistry · doi:10.1023/a:1007024126947 · Cited by 68
Peroxynitrite Formation from Activated Human Leukocytes
Fukuyama, N., Ichimori, K., Su, Z. G., Ishida, H., & Nakazawa, H. K. (1996) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1996.1041 · Cited by 67
The Quantitative Oxidation of Methionine to Methionine Sulfoxide by Peroxynitrite
Perrin, D., & Koppenol, W. H. (2000) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.2000.1787 · Cited by 67
Pietraforte, D., & Minetti, M. (1997) · Biochemical Journal · doi:10.1042/bj3210743 · Cited by 66
Peroxynitrite Isomerization Catalyzed by His64 Myoglobin Mutants
Herold, S., Matsui, T., & Watanabe, Y. (2001) · Journal of the American Chemical Society · doi:10.1021/ja010111d · Cited by 65
Formation of Spin Trap Adducts during the Decomposition of Peroxynitrite
Gatti, R. M., Álvarez, B., Vasquez-Vivar, J. M., Radí, R., & Augusto, O. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1997.0451 · Cited by 65
Oxidative Modification of Tryptophan Residues Exposed to Peroxynitrite
Kato, Y., Kawakishi, S., Aoki, T., Itakura, K., & Osawa, T. (1997) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1997.6587 · Cited by 64
Xanthine Oxidase Reaction with Nitric Oxide and Peroxynitrite
Houston, M., Chumley, P. H., Radí, R., Rubbo, H., & Freeman, B. Α. (1998) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1998.0675 · Cited by 64
The Effect of Bicarbonate on Oxidation by Peroxynitrite: Implication for Its Biological Activity
Goldstein, S., & Czapski, G. (1997) · Inorganic Chemistry · doi:10.1021/ic970471v · Cited by 62
Modulatory Role of Nitric Oxide on Superoxide-Dependent Luminol Chemiluminescence
Castro, L., Álvarez, M. N., & Radí, R. (1996) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1996.0379 · Cited by 58
Francescutti, D. M., Baldwin, J., Lee, L., & Mutus, B. (1996) · Protein Engineering Design and Selection · doi:10.1093/protein/9.2.189 · Cited by 57
Pietraforte, D., & Minetti, M. (1997) · Biochemical Journal · doi:10.1042/bj3250675 · Cited by 54
Deficiency of Myeloperoxidase Increases Infarct Volume and Nitrotyrosine Formation in Mouse Brain
Takizawa, S., Aratani, Y., Fukuyama, N., Maeda, N., Hirabayashi, H., Koyama, H., Shinohara, Y., & Nakazawa, H. K. (2002) · Journal of Cerebral Blood Flow & Metabolism · doi:10.1097/00004647-200201000-00006 · Cited by 53
Reaction of peroxynitrite with L-tryptophan
Padmaja, S., Ramazenian, M. S., Bounds, P. L., & Koppenol, W. H. (1996) · Redox Report · doi:10.1080/13510002.1996.11747045 · Cited by 53
Mallozzi, C., Stasi, M. A. M. D., & Minetti, M. (2001) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(01)00509-3 · Cited by 52
Inactivation of the Inducible Nitric Oxide Synthase by Peroxynitrite
Hühmer, A. F. R., Nishida, C. R., de Montellano, P. R. O., & Schöneich, C. (1997) · Chemical Research in Toxicology · doi:10.1021/tx960188t · Cited by 47
Ferrer‐Sueta, G., Ruíz-Azuara, L., & Radí, R. (1997) · Chemical Research in Toxicology · doi:10.1021/tx970116h · Cited by 43
Guittet, O., Ducastel, B., Salem, J. S., Henry, Y., Rubin, H., Lemaire, G., & Lepoivre, M. (1998) · Journal of Biological Chemistry · doi:10.1074/jbc.273.34.22136 · Cited by 41
Ferger, B., Themann, C., Rose, S., Halliwell, B. B., & Jenner, P. G. (2001) · Journal of Neurochemistry · doi:10.1046/j.1471-4159.2001.00429.x · Cited by 39
Forsmark-Andrée, P., Persson, B. L., Radí, R., Dallner, G., & Ernster, L. (1996) · Archives of Biochemistry and Biophysics · doi:10.1006/abbi.1996.0538 · Cited by 39
Medium effects on reactions of the carbonate radical with thiocyanate, iodide, and ferrocyanide ions
Lymar, S. V., Schwarz, H. A., & Czapski, G. (2000) · Radiation Physics and Chemistry · doi:10.1016/s0969-806x(00)00277-2 · Cited by 39
Augusto, O., de Menezes, S. L., Linares, E., Romero, N., Radí, R., & Denicola, A. (2002) · Biochemistry · doi:10.1021/bi0262202 · Cited by 35
Yangxin, F. U., Porres, J. M., & Lei, X. G. (2001) · Biochemical Journal · doi:10.1042/0264-6021:3590687 · Cited by 32
Jensen, J. L., Miller, B. L., Zhang, X., Hug, G. L., & Schöneich, C. (1997) · Journal of the American Chemical Society · doi:10.1021/ja964031z · Cited by 29
Enzymatic Reduction of 3-Nitrotyrosine Generates Superoxide
Krainev, A. G., Williams, T. D., & Bigelow, D. J. (1998) · Chemical Research in Toxicology · doi:10.1021/tx970201p · Cited by 26
Peroxynitrite-Mediated Oxidation of d,l-Selenomethionine
Padmaja, S., Squadrito, G. L., Lemercier, J.-N., Cueto, R., & Pryor, W. A. (1997) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00099-3 · Cited by 24
Oxygen-insensitive nitroreductases of Escherichia coli do not reduce 3-nitrotyrosine
Lightfoot, R. T. (2000) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(00)00208-2 · Cited by 19
O-Atom Scrambling in the Aqueous Isomerization of Pernitrous Acid
Bohle, D. S., & Hansert, B. (1997) · Nitric Oxide · doi:10.1006/niox.1997.0155 · Cited by 19
Effect of peroxynitrite on glutaredoxin
Aykaç‐Toker, G., Bulgurcuogélu, S., & Koçak‐Toker, N. (2001) · Human & Experimental Toxicology · doi:10.1191/096032701680350578 · Cited by 17
Sok, D. (1998) · Neurochemical Research · doi:10.1023/a:1020755918632 · Cited by 9
Peroxynitrite inhibits the activity of ornithine decarboxylase
Seidel, E. R., Ragan, V., & Liu, L. (2001) · Life Sciences · doi:10.1016/s0024-3205(01)00941-9 · Cited by 8
Sergeeva, S. V., Slepneva, I. A., & Khramtsov, V. V. (2001) · Free Radical Research · doi:10.1080/10715760100301501 · Cited by 7
■ Peroxynitrite biochemistry: formation, reactions and detection
Trujillo, M., Naviliat, M., Álvarez, M. N., Peluffo, G., & Radí, R. (2000) · Cited by 6
Cited by
Sorted by citations
Nitric Oxide and Peroxynitrite in Health and Disease
Pacher, P., Beckman, J. S., & Liaudet, L. (2007) · Physiological Reviews · doi:10.1152/physrev.00029.2006 · Cited by 6,390
Oxidative stress and neurodegeneration: where are we now?
Halliwell, B. (2006) · Journal of Neurochemistry · doi:10.1111/j.1471-4159.2006.03907.x · Cited by 2,614
Reactive Species and Antioxidants. Redox Biology Is a Fundamental Theme of Aerobic Life
Halliwell, B. B. (2006) · PLANT PHYSIOLOGY · doi:10.1104/pp.106.077073 · Cited by 2,402
Human serum albumin: From bench to bedside
Fanali, G., di Masi, A., Trezza, V., Marino, M., Fasano, M., & Ascenzi, P. (2011) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2011.12.002 · Cited by 2,008
Altered recognition of antigen is a mechanism of CD8+ T cell tolerance in cancer
Nagaraj, S., Gupta, K., Писарев, В. М., Kinarsky, L., Sherman, S., Kang, L., Herber, D. L., Schneck, J. P., & Gabrilovich, D. I. (2007) · Nature Medicine · doi:10.1038/nm1609 · Cited by 1,176
Metadata
- Authors
- Alvarez, B., & Radi, R.
- Venue
- Amino Acids
- Published
- 2003-09-26
- Volume
- 25
- Issue
- 3-4
- Pages
- 295-311
- ISSN
- 0939-4451 (ISSN-L)
- 1438-2199
- OpenAlex
- W2141352921
- Cited by
- 560
- References
- 147
- Citations by year
- 2026: 9 · 2025: 9 · 2024: 15 · 2023: 18 · 2022: 23 · 2021: 24 · 2020: 14 · 2019: 16 · 2018: 19 · 2017: 25 · 2016: 31 · 2015: 27 · 2014: 44 · 2013: 28 · 2012: 22
- FWCI
- 7.01
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Amino Acids (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Health Sciences › Medicine › Physiology (medical) › Nitric Oxide and Endothelin Effects
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Keywords
- peroxynitrite, nitric oxide, superoxide, protein oxidation, protein nitration, tyrosine nitration, cysteine, methionine, tryptophan, transition metal centers, selenium-containing amino acids, hydroxyl radicals, nitrogen dioxide, carbonate radical, oxidative damage
- MeSH terms
- Amino Acids, Animals, Antioxidants, Cytosol, Free Radicals, Humans, Models, Chemical, Nitric Oxide, Oxidation-Reduction, Proteins, Superoxides, Molecular Structure, Peroxynitrous Acid
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review