메뉴 건너뛰기




Volumn 18, Issue 11, 2007, Pages 2040-2057

Ammonia Elimination from Protonated Nucleobases and Related Synthetic Substrates

Author keywords

[No Author keywords available]

Indexed keywords

DENSITY FUNCTIONAL THEORY; ELECTROSPRAY IONIZATION; ION SOURCES; MASS SPECTROMETRY; PROTON TRANSFER; PROTONATION;

EID: 35448966889     PISSN: 10440305     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.jasms.2007.08.018     Document Type: Article
Times cited : (14)

References (64)
  • 1
    • 0000620153 scopus 로고
    • Reversible Denaturation of Deoxyribonucleic Acid (DNA)
    • Geiduschek E.P. Reversible Denaturation of Deoxyribonucleic Acid (DNA). Proc. Natl. Acad. Sci. U.S.A. 47 (1961) 950-955
    • (1961) Proc. Natl. Acad. Sci. U.S.A. , vol.47 , pp. 950-955
    • Geiduschek, E.P.1
  • 2
    • 0000289783 scopus 로고
    • On the Factors Controlling the Reversibility of DNA Denaturation
    • Geiduschek E.P. On the Factors Controlling the Reversibility of DNA Denaturation. J. Mol. Biol. 4 (1962) 467-487
    • (1962) J. Mol. Biol. , vol.4 , pp. 467-487
    • Geiduschek, E.P.1
  • 4
    • 0003526345 scopus 로고
    • Committee on Nitrite and Alternative Curing Agents in Food, National Academy Press, Washington, D.C
    • Committee on Nitrite and Alternative Curing Agents in Food. The Health Effect of Nitrate, Nitrite, and N-Nitroso Compounds (1981), National Academy Press, Washington, D.C
    • (1981) The Health Effect of Nitrate, Nitrite, and N-Nitroso Compounds
  • 7
    • 0027080129 scopus 로고
    • No News is Good News
    • Culotta E., and Koshland D.E. No News is Good News. Science 258 (1992) 1862-1865
    • (1992) Science , vol.258 , pp. 1862-1865
    • Culotta, E.1    Koshland, D.E.2
  • 8
    • 0029682434 scopus 로고    scopus 로고
    • Nitric Oxide: Chemical Events in Toxicity
    • Marnett L.J. Nitric Oxide: Chemical Events in Toxicity. Chem. Res. Toxicol. 9 (1996) 807-808
    • (1996) Chem. Res. Toxicol. , vol.9 , pp. 807-808
    • Marnett, L.J.1
  • 10
    • 0035796023 scopus 로고    scopus 로고
    • The Contribution of Endogenous Sources of DNA Damage to the Multiple Mutations in Cancer
    • Jackson A.L., and Loeb L.A. The Contribution of Endogenous Sources of DNA Damage to the Multiple Mutations in Cancer. Mutat. Res. 477 (2001) 7-21
    • (2001) Mutat. Res. , vol.477 , pp. 7-21
    • Jackson, A.L.1    Loeb, L.A.2
  • 11
    • 0028218474 scopus 로고
    • Chronic Infections and Inflammatory Processes as Cancer Risk Factors: Possible Role of Nitric Oxide in Carcinogenesis
    • Ohshima H., and Bartsch H. Chronic Infections and Inflammatory Processes as Cancer Risk Factors: Possible Role of Nitric Oxide in Carcinogenesis. Mutat. Res. 305 (1994) 253-264
    • (1994) Mutat. Res. , vol.305 , pp. 253-264
    • Ohshima, H.1    Bartsch, H.2
  • 12
    • 0030577116 scopus 로고    scopus 로고
    • The Role of Nitric Oxide (NO) in the Carcinogenic Process.
    • Tamir S., and Tannenbaum S.R. The Role of Nitric Oxide (NO) in the Carcinogenic Process. Biochim. Biophys. Acta 1288 (1996) F31-F36
    • (1996) Biochim. Biophys. Acta , vol.1288
    • Tamir, S.1    Tannenbaum, S.R.2
  • 13
    • 0034650196 scopus 로고    scopus 로고
    • Formation of 2′-Deoxyoxanosine from 2′-Deoxyguanosine and Nitrous Acid: Mechanism and Intermediates
    • Suzuki T., Ide H., Yamada M., Endo N., Kanaori K., Tajima K., Morii T., and Makino K. Formation of 2′-Deoxyoxanosine from 2′-Deoxyguanosine and Nitrous Acid: Mechanism and Intermediates. Nucleic Acids Res 28 (2000) 544-551
    • (2000) Nucleic Acids Res , vol.28 , pp. 544-551
    • Suzuki, T.1    Ide, H.2    Yamada, M.3    Endo, N.4    Kanaori, K.5    Tajima, K.6    Morii, T.7    Makino, K.8
  • 14
    • 0033603420 scopus 로고    scopus 로고
    • Efficient Nitroso Group Transfer from N-Nitrosoindoles to Nucleotides and 2′-Deoxyguanosine at Physiological pH. A New Pathway for N-Nitroso Compounds to Exert Genotoxicity
    • Lucas L.T., Gatehouse D., and Shuker D.E.G. Efficient Nitroso Group Transfer from N-Nitrosoindoles to Nucleotides and 2′-Deoxyguanosine at Physiological pH. A New Pathway for N-Nitroso Compounds to Exert Genotoxicity. J. Biol. Chem. 274 (1999) 18319-18326
    • (1999) J. Biol. Chem. , vol.274 , pp. 18319-18326
    • Lucas, L.T.1    Gatehouse, D.2    Shuker, D.E.G.3
  • 15
    • 0141848395 scopus 로고    scopus 로고
    • Absence of 2′-Deoxyoxanosine and Presence of Abasic Sites in DNA Exposed to Nitric Oxide at Controlled Physiological Concentrations
    • Dong M., Wang C., Deen W.M., and Dedon P.C. Absence of 2′-Deoxyoxanosine and Presence of Abasic Sites in DNA Exposed to Nitric Oxide at Controlled Physiological Concentrations. Chem. Res. Toxicol. 16 (2003) 1044-1055
    • (2003) Chem. Res. Toxicol. , vol.16 , pp. 1044-1055
    • Dong, M.1    Wang, C.2    Deen, W.M.3    Dedon, P.C.4
  • 16
    • 0029849366 scopus 로고    scopus 로고
    • Pyrimidine Ring Opening in the Unimolecular Dediazoniation of Guanine Diazonium Ion. An ab Initio Theoretical Study of the Mechanism of Nitrosative Guanosine Deamination
    • Glaser R., and Son M.-S. Pyrimidine Ring Opening in the Unimolecular Dediazoniation of Guanine Diazonium Ion. An ab Initio Theoretical Study of the Mechanism of Nitrosative Guanosine Deamination. J. Am. Chem. Soc. 118 (1996) 10942-10943
    • (1996) J. Am. Chem. Soc. , vol.118 , pp. 10942-10943
    • Glaser, R.1    Son, M.-S.2
  • 17
    • 0033532945 scopus 로고    scopus 로고
    • Theoretical Studies of DNA Base Deamination. 2. Ab Initio Study of DNA Base Diazonium Ions and of Their Linear, Unimolecular Dediazoniation Paths
    • Glaser R., Rayat S., Lewis M., Son M.-S., and Meyer S. Theoretical Studies of DNA Base Deamination. 2. Ab Initio Study of DNA Base Diazonium Ions and of Their Linear, Unimolecular Dediazoniation Paths. J. Am. Chem. Soc. 121 (1999) 6108-6119
    • (1999) J. Am. Chem. Soc. , vol.121 , pp. 6108-6119
    • Glaser, R.1    Rayat, S.2    Lewis, M.3    Son, M.-S.4    Meyer, S.5
  • 18
    • 0033614862 scopus 로고    scopus 로고
    • Single- and Double-Proton-Transfer in the Aggregate Between Cytosine and Guaninediazonium Ion
    • Glaser R., and Lewis M. Single- and Double-Proton-Transfer in the Aggregate Between Cytosine and Guaninediazonium Ion. Org. Lett. 1 (1999) 273-276
    • (1999) Org. Lett. , vol.1 , pp. 273-276
    • Glaser, R.1    Lewis, M.2
  • 19
    • 19744377792 scopus 로고    scopus 로고
    • Cytosine Catalysis of Nitrosative Guanine Deamination and Interstrand Cross-Link Formation
    • Glaser R., Wu H., and Lewis M. Cytosine Catalysis of Nitrosative Guanine Deamination and Interstrand Cross-Link Formation. J. Am. Chem. Soc. 127 (2005) 7346-7358
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 7346-7358
    • Glaser, R.1    Wu, H.2    Lewis, M.3
  • 20
    • 0347624002 scopus 로고    scopus 로고
    • 5-Cyanoimino-4-Oxomethylene-dihydroimidazole and Nitrosative Guanine Deamination. A Theoretical Study of Geometries, Electronic Structures, and N-Protonation
    • Rayat S., and Glaser R. 5-Cyanoimino-4-Oxomethylene-dihydroimidazole and Nitrosative Guanine Deamination. A Theoretical Study of Geometries, Electronic Structures, and N-Protonation. J. Org. Chem. 68 (2003) 9882-9892
    • (2003) J. Org. Chem. , vol.68 , pp. 9882-9892
    • Rayat, S.1    Glaser, R.2
  • 21
    • 4043059199 scopus 로고    scopus 로고
    • 5-Cyanoimino-4-Oxomethylene-4,5-Dihydroimidazole and 5-Cyanoamino-4-Imidazolecarboxylic Acid Intermediates in Nitrosative Guanosine Deamination. Evidence from (18)O-Labeling Experiments
    • Rayat S., Majumdar P., Tipton P., and Glaser R. 5-Cyanoimino-4-Oxomethylene-4,5-Dihydroimidazole and 5-Cyanoamino-4-Imidazolecarboxylic Acid Intermediates in Nitrosative Guanosine Deamination. Evidence from (18)O-Labeling Experiments. J. Am. Chem. Soc. 126 (2004) 9960-9969
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 9960-9969
    • Rayat, S.1    Majumdar, P.2    Tipton, P.3    Glaser, R.4
  • 22
    • 1542375033 scopus 로고    scopus 로고
    • 5-Cyanoamino-4-Imidazolecarboxamide and Nitrosative Guanine Deamination: Experimental Evidence for Pyrimidine Ring-Opening During Deamination
    • Qian M., and Glaser R. 5-Cyanoamino-4-Imidazolecarboxamide and Nitrosative Guanine Deamination: Experimental Evidence for Pyrimidine Ring-Opening During Deamination. J. Am. Chem. Soc. 126 (2004) 2274-2275
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 2274-2275
    • Qian, M.1    Glaser, R.2
  • 23
    • 12444327229 scopus 로고    scopus 로고
    • Demonstration of an Alternative Mechanism for G-to-G Cross-Link Formation
    • Qian M., and Glaser R. Demonstration of an Alternative Mechanism for G-to-G Cross-Link Formation. J. Am. Chem. Soc. 127 (2005) 880-887
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 880-887
    • Qian, M.1    Glaser, R.2
  • 24
    • 0344514169 scopus 로고    scopus 로고
    • Nitrosative Adenine Deamination: Facile Pyrimidine Ring-Opening in the Dediazoniation of Adeninediazonium Ion
    • Hodgen B., Rayat S., and Glaser R. Nitrosative Adenine Deamination: Facile Pyrimidine Ring-Opening in the Dediazoniation of Adeninediazonium Ion. Org. Lett. 5 (2003) 4077-4080
    • (2003) Org. Lett. , vol.5 , pp. 4077-4080
    • Hodgen, B.1    Rayat, S.2    Glaser, R.3
  • 28
  • 30
    • 0014215579 scopus 로고
    • Mass Spectra of Nucleic Acid Derivatives. II. Guanine, Adenine, and Related Compounds
    • Rice J.M., and Dudek G.O. Mass Spectra of Nucleic Acid Derivatives. II. Guanine, Adenine, and Related Compounds. J. Am. Chem. Soc. 89 (1967) 2719-2725
    • (1967) J. Am. Chem. Soc. , vol.89 , pp. 2719-2725
    • Rice, J.M.1    Dudek, G.O.2
  • 32
    • 0000235005 scopus 로고
    • Mass Spectrometry of Nucleic Acid Constituents. Electron Ionization Spectra of Selectively Labeled Adenines
    • Sethi S.K., Gupta S.P., Jenkins E.E., Whitehead C.W., Townsend L.B., and McCloskey J.A. Mass Spectrometry of Nucleic Acid Constituents. Electron Ionization Spectra of Selectively Labeled Adenines. J. Am. Chem. Soc. 104 (1982) 3349-3353
    • (1982) J. Am. Chem. Soc. , vol.104 , pp. 3349-3353
    • Sethi, S.K.1    Gupta, S.P.2    Jenkins, E.E.3    Whitehead, C.W.4    Townsend, L.B.5    McCloskey, J.A.6
  • 33
    • 0013851652 scopus 로고
    • Mass Spectra of Nucleic Acid Derivatives Pyrimidines
    • Rice J.M., Dudek G.O., and Barber M. Mass Spectra of Nucleic Acid Derivatives Pyrimidines. J. Am. Chem. Soc. 87 (1965) 4569-4576
    • (1965) J. Am. Chem. Soc. , vol.87 , pp. 4569-4576
    • Rice, J.M.1    Dudek, G.O.2    Barber, M.3
  • 34
    • 0344027285 scopus 로고    scopus 로고
    • Atmospheric Pressure Ionization Mass Spectrometry of Purine and Pyrimidine Markers of Inherited Metabolic Disorders
    • Fryèák P., HušKová R., Tomáš A., and Lemr K. Atmospheric Pressure Ionization Mass Spectrometry of Purine and Pyrimidine Markers of Inherited Metabolic Disorders. J. Mass Spectrom. 37 (2002) 1242-1248
    • (2002) J. Mass Spectrom. , vol.37 , pp. 1242-1248
    • Fryèák, P.1    HušKová, R.2    Tomáš, A.3    Lemr, K.4
  • 35
    • 0016838666 scopus 로고
    • Chemical ionization mass spectrometry of nucleosides. Mechanisms of ion formation and estimations of proton affinity
    • Wilson M.S., and McCloskey J.A. Chemical ionization mass spectrometry of nucleosides. Mechanisms of ion formation and estimations of proton affinity. J. Am. Chem. Soc. 97 (1975) 3436-3444
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 3436-3444
    • Wilson, M.S.1    McCloskey, J.A.2
  • 36
    • 0026773531 scopus 로고
    • Collision-Induced Dissociation of Adenine
    • Nelson C.C., and McCloskey J.A. Collision-Induced Dissociation of Adenine. J. Am. Chem. Soc. 114 (1992) 3661-3668
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 3661-3668
    • Nelson, C.C.1    McCloskey, J.A.2
  • 38
    • 27944474245 scopus 로고    scopus 로고
    • Gas-phase tautomers of protonated 1-methylcytosine. Preparation, energetics, and dissociation mechanisms
    • Yao C., Cuadrado-Peinado M.L., Polasek M., and Tureček F. Gas-phase tautomers of protonated 1-methylcytosine. Preparation, energetics, and dissociation mechanisms. J. Mass Spectrom. 40 (2005) 1417-1428
    • (2005) J. Mass Spectrom. , vol.40 , pp. 1417-1428
    • Yao, C.1    Cuadrado-Peinado, M.L.2    Polasek, M.3    Tureček, F.4
  • 39
    • 34250788545 scopus 로고    scopus 로고
    • Proton and hydrogen atom adducts to cytosine. An experimental and computational study
    • Yao C., Tureček F., Polce M.J., and Wesdemiotis C. Proton and hydrogen atom adducts to cytosine. An experimental and computational study. Int. J. Mass Spectrom. 265 (2007) 106-123
    • (2007) Int. J. Mass Spectrom. , vol.265 , pp. 106-123
    • Yao, C.1    Tureček, F.2    Polce, M.J.3    Wesdemiotis, C.4
  • 40
    • 33748956160 scopus 로고    scopus 로고
    • Collisionally Activated Dissociation of Protonated 2'-Deoxycytidine, 2'-Deoxyuridine, and their Oxidatively Damaged Derivatives
    • Cao H., and Wang Y. Collisionally Activated Dissociation of Protonated 2'-Deoxycytidine, 2'-Deoxyuridine, and their Oxidatively Damaged Derivatives. J. Am. Soc. Mass. Spectrom. 17 (2006) 1335-1341
    • (2006) J. Am. Soc. Mass. Spectrom. , vol.17 , pp. 1335-1341
    • Cao, H.1    Wang, Y.2
  • 41
    • 25144492004 scopus 로고    scopus 로고
    • Protonated Adenine: Tautomers, Solvated Clusters, and Dissociation Mechanisms
    • Tureček F., and Chen X. Protonated Adenine: Tautomers, Solvated Clusters, and Dissociation Mechanisms. J. Am. Soc. Mass Spectrom. 16 (2005) 1713-1726
    • (2005) J. Am. Soc. Mass Spectrom. , vol.16 , pp. 1713-1726
    • Tureček, F.1    Chen, X.2
  • 42
    • 0034422658 scopus 로고    scopus 로고
    • Theoretical Methods for Computing Enthalpies of Formation of Gaseous Compounds
    • Curtiss L.A., Redfern P.C., and Frurip D.J. Theoretical Methods for Computing Enthalpies of Formation of Gaseous Compounds. Rev. Comput. Chem. 15 (2000) 147-211
    • (2000) Rev. Comput. Chem. , vol.15 , pp. 147-211
    • Curtiss, L.A.1    Redfern, P.C.2    Frurip, D.J.3
  • 43
    • 0036399323 scopus 로고    scopus 로고
    • Density Functional Theoretical (DFT) and Surface-Enhanced Raman Spectroscopic Study of Guanine and Its Alkylated Derivatives. Part 1. DFT Calculations on Neutral, Protonated, and Deprotonated Guanine
    • Giese B., and McNaughton D. Density Functional Theoretical (DFT) and Surface-Enhanced Raman Spectroscopic Study of Guanine and Its Alkylated Derivatives. Part 1. DFT Calculations on Neutral, Protonated, and Deprotonated Guanine. Phys. Chem. Chem. Phys. 4 (2002) 5161-5170
    • (2002) Phys. Chem. Chem. Phys. , vol.4 , pp. 5161-5170
    • Giese, B.1    McNaughton, D.2
  • 45
    • 0025596909 scopus 로고
    • Gas-Phase Proton Affinity of Deoxyribonucleosides and Related Nucleobases by Fast Atom Bombardment Tandem Mass Spectrometry
    • Greco F., Liguori A., Sindona G., and Uccella N. Gas-Phase Proton Affinity of Deoxyribonucleosides and Related Nucleobases by Fast Atom Bombardment Tandem Mass Spectrometry. J. Am. Chem. Soc. 112 (1990) 9092-9096
    • (1990) J. Am. Chem. Soc. , vol.112 , pp. 9092-9096
    • Greco, F.1    Liguori, A.2    Sindona, G.3    Uccella, N.4
  • 46
    • 0001394051 scopus 로고    scopus 로고
    • Protonation and Deprotonation Enthalpies of Guanine and Adenine and Implications for the Structure and Energy of Their Complexes with Water: Comparison with Uracil, Thymine, and Cytosine
    • Chandra A.K., Nguyen M.T., Uchimaru T., and Zeegers-Huyskens T. Protonation and Deprotonation Enthalpies of Guanine and Adenine and Implications for the Structure and Energy of Their Complexes with Water: Comparison with Uracil, Thymine, and Cytosine. J. Phys. Chem. A 103 (1999) 8853-8860
    • (1999) J. Phys. Chem. A , vol.103 , pp. 8853-8860
    • Chandra, A.K.1    Nguyen, M.T.2    Uchimaru, T.3    Zeegers-Huyskens, T.4
  • 47
    • 0003946118 scopus 로고
    • Caldin E.F., and Gold V. (Eds), Wiley-Halstead, New York Chap II
    • Taft R.W. Proton Transfer Reaction. In: Caldin E.F., and Gold V. (Eds) (1975), Wiley-Halstead, New York Chap II
    • (1975) Proton Transfer Reaction
    • Taft, R.W.1
  • 49
    • 0001199658 scopus 로고
    • An Ion Mobility Spectrometry/Mass Spectrometry (IMS/MS) Study of the Site of Protonation in Anilines
    • Karpas Z., Berant Z., and Stimac R.M. An Ion Mobility Spectrometry/Mass Spectrometry (IMS/MS) Study of the Site of Protonation in Anilines. Struct. Chem. 1 (1990) 201-204
    • (1990) Struct. Chem. , vol.1 , pp. 201-204
    • Karpas, Z.1    Berant, Z.2    Stimac, R.M.3
  • 51
    • 33746332072 scopus 로고    scopus 로고
    • Dissociative Protonation Sites: Reactive Centers in Protonated Molecules Leading to Fragmentation in Mass Spectrometry
    • Tu Y.-P. Dissociative Protonation Sites: Reactive Centers in Protonated Molecules Leading to Fragmentation in Mass Spectrometry. J. Org. Chem. 71 (2006) 5482-5488
    • (2006) J. Org. Chem. , vol.71 , pp. 5482-5488
    • Tu, Y.-P.1
  • 52
    • 21844457685 scopus 로고    scopus 로고
    • Fragmentation Pathways of Protonated Peptides
    • Paizs B., and Suhai S. Fragmentation Pathways of Protonated Peptides. Mass Spectrom. Rev. 24 (2005) 508-548
    • (2005) Mass Spectrom. Rev. , vol.24 , pp. 508-548
    • Paizs, B.1    Suhai, S.2
  • 54
    • 4544265129 scopus 로고    scopus 로고
    • Modeling of the Gas-Phase Ion Chemistry of Protonated Arginine
    • Csonka I.P., Paizs B., and Suhai S. Modeling of the Gas-Phase Ion Chemistry of Protonated Arginine. J. Mass Spectrom. 39 (2004) 1025-1035
    • (2004) J. Mass Spectrom. , vol.39 , pp. 1025-1035
    • Csonka, I.P.1    Paizs, B.2    Suhai, S.3
  • 55
    • 33751313863 scopus 로고    scopus 로고
    • Isotope Labeling and Theoretical Study of the Formation of a3* Ions from Protonated Tetraglycine
    • Cooper T., Talaty E., Grove J., Van Stipdonk M., Suhai S., and Paizs B. Isotope Labeling and Theoretical Study of the Formation of a3* Ions from Protonated Tetraglycine. J. Am. Soc. Mass Spectrom. 17 (2006) 1654-1664
    • (2006) J. Am. Soc. Mass Spectrom. , vol.17 , pp. 1654-1664
    • Cooper, T.1    Talaty, E.2    Grove, J.3    Van Stipdonk, M.4    Suhai, S.5    Paizs, B.6
  • 56
    • 34547744326 scopus 로고    scopus 로고
    • Adenine Synthesis in Interstellar Space: Mechanisms of Prebiotic Pyrimidine Ring-Formation in Monocyclic HCN-Pentamers
    • Glaser R., Hodgen B., Farrelly D., and McKee E. Adenine Synthesis in Interstellar Space: Mechanisms of Prebiotic Pyrimidine Ring-Formation in Monocyclic HCN-Pentamers. Astrobiology 7 (2007) 455-470
    • (2007) Astrobiology , vol.7 , pp. 455-470
    • Glaser, R.1    Hodgen, B.2    Farrelly, D.3    McKee, E.4
  • 57
    • 33645557037 scopus 로고    scopus 로고
    • Reaction mechanisms. Part III. Pericyclic reactions
    • Morgan K.M. Reaction mechanisms. Part III. Pericyclic reactions. Annu. Rep. Prog. Chem. B 101 (2005) 284-304
    • (2005) Annu. Rep. Prog. Chem. B , vol.101 , pp. 284-304
    • Morgan, K.M.1
  • 60
    • 0000131701 scopus 로고
    • Unimolecular Chemistry of Protonated Formamide. Mass Spectrometry and ab Initio Quantum Chemical Calculations
    • Lin H.Y., Ridge D.P., Uggerud E., and Vulpius T. Unimolecular Chemistry of Protonated Formamide. Mass Spectrometry and ab Initio Quantum Chemical Calculations. J. Am. Chem. Soc. 116 (1994) 2996-3004
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 2996-3004
    • Lin, H.Y.1    Ridge, D.P.2    Uggerud, E.3    Vulpius, T.4
  • 62
    • 0000397152 scopus 로고
    • Mass Spectrometric Determination of the Proton Affinities of Various Molecules
    • Haney M.A., and Franklin J.L. Mass Spectrometric Determination of the Proton Affinities of Various Molecules. J. Phys. Chem. 73 (1969) 4328-4331
    • (1969) J. Phys. Chem. , vol.73 , pp. 4328-4331
    • Haney, M.A.1    Franklin, J.L.2
  • 63
    • 33746419616 scopus 로고    scopus 로고
    • Chemical Carcinogens in Nonenzymatic Cytosine Deamination: 3-Isocyanatoacrylonitrile
    • Glaser R., Wu H., and von Saint Paul F. Chemical Carcinogens in Nonenzymatic Cytosine Deamination: 3-Isocyanatoacrylonitrile. J. Mol. Model 12 (2006) 731-737
    • (2006) J. Mol. Model , vol.12 , pp. 731-737
    • Glaser, R.1    Wu, H.2    von Saint Paul, F.3
  • 64
    • 14744299376 scopus 로고    scopus 로고
    • The Role of Electron Capture Dissociation in Biomolecular Analysis
    • Cooper H.J., Hakansson K., and Marshall A.G. The Role of Electron Capture Dissociation in Biomolecular Analysis. Mass Spectrom. Rev. 24 (2005) 201-222
    • (2005) Mass Spectrom. Rev. , vol.24 , pp. 201-222
    • Cooper, H.J.1    Hakansson, K.2    Marshall, A.G.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.