메뉴 건너뛰기




Volumn 43, Issue 8, 2008, Pages 1132-1139

Mechanism of a gas-phase dissociation reaction of 4-aminobutyl glycosides under CID MS/MS conditions

Author keywords

Aminobutyl; C ion; CID; ERMS; Glycosides; Reaction mechanism

Indexed keywords

ARSENIC COMPOUNDS; CHLORINE COMPOUNDS; COMPLEXATION; GLUCOSE; HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; MASS SPECTROMETERS; MASS SPECTROMETRY; MECHANISMS; SPECTROMETERS; SPECTROMETRY; SPECTRUM ANALYSIS; STRUCTURAL ANALYSIS; SUGARS;

EID: 49549093417     PISSN: 10765174     EISSN: 10969888     Source Type: Journal    
DOI: 10.1002/jms.1397     Document Type: Article
Times cited : (4)

References (39)
  • 2
    • 34248592487 scopus 로고    scopus 로고
    • Detection of attomole amounts of analyte by desorption electrospray ionization mass spectrometry (DESI-MS) determined using fluorescence spectroscopy
    • Bereman MS, Muddiman DC. Detection of attomole amounts of analyte by desorption electrospray ionization mass spectrometry (DESI-MS) determined using fluorescence spectroscopy. Journal of the American Society for Mass Spectrometry 2007; 18: 1093.
    • (2007) Journal of the American Society for Mass Spectrometry , vol.18 , pp. 1093
    • Bereman, M.S.1    Muddiman, D.C.2
  • 3
    • 0028607322 scopus 로고    scopus 로고
    • 12 structures for a reducing hexasaccharide: The isomer barrier to development of single-method saccharide sequencing or synthesis systems. Glycobiology 1994; 4: 759.
    • 12 structures for a reducing hexasaccharide: The isomer barrier to development of single-method saccharide sequencing or synthesis systems. Glycobiology 1994; 4: 759.
  • 4
    • 0032846691 scopus 로고    scopus 로고
    • Enzymatic glycosylation of reducing oligosaccharides linked to a solid phase or a lipid via a cleavable squarate linker
    • Blixt O, Norberg T. Enzymatic glycosylation of reducing oligosaccharides linked to a solid phase or a lipid via a cleavable squarate linker. Carbohydrate Research 1999; 319: 80.
    • (1999) Carbohydrate Research , vol.319 , pp. 80
    • Blixt, O.1    Norberg, T.2
  • 6
    • 0036232915 scopus 로고    scopus 로고
    • Carbohydrate arrays for the evaluation of protein binding and enzymatic modification
    • Houseman BT, Mrksich M. Carbohydrate arrays for the evaluation of protein binding and enzymatic modification. Chemistry and Biology 2002; 9: 443.
    • (2002) Chemistry and Biology , vol.9 , pp. 443
    • Houseman, B.T.1    Mrksich, M.2
  • 7
    • 0141995591 scopus 로고    scopus 로고
    • A new kind of carbohydrate array, its use for profiling antiglycan antibodies, and the discovery of a novel human cellulose-binding antibody
    • Schwarz M, Spector L, Gargir A, Shtevi A, Gortler M, Altstock RT, Dukler AA, Dotan N. A new kind of carbohydrate array, its use for profiling antiglycan antibodies, and the discovery of a novel human cellulose-binding antibody. Glycobiology 2003; 13: 749.
    • (2003) Glycobiology , vol.13 , pp. 749
    • Schwarz, M.1    Spector, L.2    Gargir, A.3    Shtevi, A.4    Gortler, M.5    Altstock, R.T.6    Dukler, A.A.7    Dotan, N.8
  • 10
    • 0030982767 scopus 로고    scopus 로고
    • Structural requirements of Rhizobium chitolipooligosaccharides for uptake and bioactivity in legume roots as revealed by synthetic analogs and fluorescent probes
    • Philip-Hollingsworth S, Dazzo FB, Hollingsworth RI. Hollingsworth RI. Structural requirements of Rhizobium chitolipooligosaccharides for uptake and bioactivity in legume roots as revealed by synthetic analogs and fluorescent probes. Journal of Lipid Research 1997; 38: 1229.
    • (1997) Journal of Lipid Research , vol.38 , pp. 1229
    • Philip-Hollingsworth, S.1    Dazzo, F.B.2    Hollingsworth, R.I.3    Hollingsworth, R.I.4
  • 12
    • 0025691545 scopus 로고
    • Collision-induced dissociation
    • ed, Academic press: Sandiego;
    • Hayes RN, Gross ML. Collision-induced dissociation. In Method Enzymol. McCloskey JA (ed), vol. 193, Academic press: Sandiego; 1990; 237.
    • (1990) Method Enzymol , vol.193 , pp. 237
    • Hayes, R.N.1    Gross, M.L.2
  • 13
    • 0035937542 scopus 로고    scopus 로고
    • Glycoprotein structure determination by mass spectrometry
    • Dell A, Morris HR. Glycoprotein structure determination by mass spectrometry. Science 2001; 291: 2351.
    • (2001) Science , vol.291 , pp. 2351
    • Dell, A.1    Morris, H.R.2
  • 14
    • 0032402250 scopus 로고    scopus 로고
    • Structural assignment of permethylated oligosaccharide subunits using sequential tandem mass spectrometry
    • Viseux N, de Hoffmann E, Domon B. Structural assignment of permethylated oligosaccharide subunits using sequential tandem mass spectrometry. Analytical Chemistry 1998; 70: 4951.
    • (1998) Analytical Chemistry , vol.70 , pp. 4951
    • Viseux, N.1    de Hoffmann, E.2    Domon, B.3
  • 20
    • 0040317079 scopus 로고    scopus 로고
    • Determination of linkage position and anomeric configuration in glucose-containing disaccharide alditols by multivariate analysis of data from mass spectrometry
    • Fängmark I, Jansson A, Nilsson B. Determination of linkage position and anomeric configuration in glucose-containing disaccharide alditols by multivariate analysis of data from mass spectrometry. Analytical Chemistry 1999; 71: 1105.
    • (1999) Analytical Chemistry , vol.71 , pp. 1105
    • Fängmark, I.1    Jansson, A.2    Nilsson, B.3
  • 21
    • 0028058714 scopus 로고
    • Differentiation of isomeric alditol hexaacetates and identification of aldohexoses by electron impact mass spectrometry
    • Higgins MK, Bly RS, Morgan SL. Differentiation of isomeric alditol hexaacetates and identification of aldohexoses by electron impact mass spectrometry. Analytical Chemistry 1994; 66: 2656.
    • (1994) Analytical Chemistry , vol.66 , pp. 2656
    • Higgins, M.K.1    Bly, R.S.2    Morgan, S.L.3
  • 23
    • 27944474358 scopus 로고    scopus 로고
    • Single-step multisyntheses of glycosyl acceptors: Benzylation of n-1 hydroxyl groups of phenylthio glycosides of xylose, mannose, glucose, galactose, 2-azido-2-deoxy-glucose, and 2-azido-2-deoxy-galactose
    • Suzuki K, Ohtsuka I, Kanemitsu T, Ako T, Kanie O. Single-step multisyntheses of glycosyl acceptors: Benzylation of n-1 hydroxyl groups of phenylthio glycosides of xylose, mannose, glucose, galactose, 2-azido-2-deoxy-glucose, and 2-azido-2-deoxy-galactose. Journal of Carbohydrate Chemistry 2005; 24: 219.
    • (2005) Journal of Carbohydrate Chemistry , vol.24 , pp. 219
    • Suzuki, K.1    Ohtsuka, I.2    Kanemitsu, T.3    Ako, T.4    Kanie, O.5
  • 24
    • 33746265839 scopus 로고    scopus 로고
    • Orthogonal glycosylation reactions on solid phase and synthesis of a library consisting of a complete set of fucosyl galactose isomers
    • Kanie O, Ohtsuka I, Ako T, Daikoku S, Kanie Y, Kato R. Orthogonal glycosylation reactions on solid phase and synthesis of a library consisting of a complete set of fucosyl galactose isomers. Angewandte Chemie International Edition 2006; 45: 3851.
    • (2006) Angewandte Chemie International Edition , vol.45 , pp. 3851
    • Kanie, O.1    Ohtsuka, I.2    Ako, T.3    Daikoku, S.4    Kanie, Y.5    Kato, R.6
  • 25
    • 33646919889 scopus 로고    scopus 로고
    • Synthesis of a library of fucopyranosylgalactopyranosides consisting of a complete set of anomeric configurations and linkage positions
    • Ohtsuka I, Ako T, Kato R, Daikoku S, Koroghi S, Kanemitsu T, Kanie O. Synthesis of a library of fucopyranosylgalactopyranosides consisting of a complete set of anomeric configurations and linkage positions. Carbohydrate Research 2006; 341: 1476.
    • (2006) Carbohydrate Research , vol.341 , pp. 1476
    • Ohtsuka, I.1    Ako, T.2    Kato, R.3    Daikoku, S.4    Koroghi, S.5    Kanemitsu, T.6    Kanie, O.7
  • 27
    • 33845945191 scopus 로고    scopus 로고
    • A method of orthogonal oligosaccharide synthesis leading to a combinatorial library based on stationary solid-phase reaction
    • Ako T, Daikoku S, Ohtsuka I, Kato R, Kanie O. A method of orthogonal oligosaccharide synthesis leading to a combinatorial library based on stationary solid-phase reaction. Chemistry - An Asian Journal 2006; 1: 798.
    • (2006) Chemistry - An Asian Journal , vol.1 , pp. 798
    • Ako, T.1    Daikoku, S.2    Ohtsuka, I.3    Kato, R.4    Kanie, O.5
  • 28
    • 0001384408 scopus 로고    scopus 로고
    • Laine RA, Pamidimukkala KM, French AD, Hall RW, Abbas SA, Jain RK, Matta KL. Linkage position in oligosaccharides by fast atom bombardment ionization, collision-activated dissociation, tandem mass spectrometry and molecular modeling. L-fucosylp-(α1 → X)-D-N- acetyl-D-glucosaminylp-(β1 → 3)-D- galactosylp-(β1-O-methyl) where X = 3, 4, or 6. Journal of the American Chemical Society 1988; 110: 6931.
    • Laine RA, Pamidimukkala KM, French AD, Hall RW, Abbas SA, Jain RK, Matta KL. Linkage position in oligosaccharides by fast atom bombardment ionization, collision-activated dissociation, tandem mass spectrometry and molecular modeling. L-fucosylp-(α1 → X)-D-N- acetyl-D-glucosaminylp-(β1 → 3)-D- galactosylp-(β1-O-methyl) where X = 3, 4, or 6. Journal of the American Chemical Society 1988; 110: 6931.
  • 31
    • 34250877855 scopus 로고    scopus 로고
    • Anomeric information obtained from a series of synthetic trisaccharides using energy resolved mass spectra
    • Daikoku S, Ako T, Kurimoto A, Kanie O. Anomeric information obtained from a series of synthetic trisaccharides using energy resolved mass spectra. Journal of Mass Spectrometry 2007; 42: 714.
    • (2007) Journal of Mass Spectrometry , vol.42 , pp. 714
    • Daikoku, S.1    Ako, T.2    Kurimoto, A.3    Kanie, O.4
  • 33
    • 0026942153 scopus 로고
    • Linkage position determination in a novel set of permethylated neutral trisaccharides by collisional-induced dissociation and tandem mass spectrometry
    • Yoon E, Lain RA. Linkage position determination in a novel set of permethylated neutral trisaccharides by collisional-induced dissociation and tandem mass spectrometry. Biological Mass Spectrometry 1992; 21: 479.
    • (1992) Biological Mass Spectrometry , vol.21 , pp. 479
    • Yoon, E.1    Lain, R.A.2
  • 34
    • 0026222526 scopus 로고
    • Non-reducing terminal linkage position determination in intact and permethylated synthetic oligosaccharides having a penultimate amino sugar: Fast atom bombardment ionization, collisional-induced dissociation and tandem mass spectrometry
    • Lain RA, Yoon E, Mahier TJ, Abbas S, de Lappe B, Jain R, Matta K. Non-reducing terminal linkage position determination in intact and permethylated synthetic oligosaccharides having a penultimate amino sugar: Fast atom bombardment ionization, collisional-induced dissociation and tandem mass spectrometry. Biological Mass Spectrometry 1991; 20: 505.
    • (1991) Biological Mass Spectrometry , vol.20 , pp. 505
    • Lain, R.A.1    Yoon, E.2    Mahier, T.J.3    Abbas, S.4    de Lappe, B.5    Jain, R.6    Matta, K.7
  • 35
    • 34547909916 scopus 로고    scopus 로고
    • Distinguishing isomeric pyridylaminated high-mannose (Man7) oligosaccharides based on energy-resolved mass spectra
    • Kurimoto A, Kanie O. Distinguishing isomeric pyridylaminated high-mannose (Man7) oligosaccharides based on energy-resolved mass spectra. Rapid Communications in Mass Spectrometry 2007; 21: 2770.
    • (2007) Rapid Communications in Mass Spectrometry , vol.21 , pp. 2770
    • Kurimoto, A.1    Kanie, O.2
  • 36
    • 36848999868 scopus 로고    scopus 로고
    • High-yielding and controlled dissociation of glycosides producing B- and C-ion species under collision-induced dissociation MS/MS conditions and use in structural determination
    • Suzuki K, Daikoku S, Ako T, Kurimoto A, Ohtake A, Shioiri Y, Sarkar SK, Kanie O. High-yielding and controlled dissociation of glycosides producing B- and C-ion species under collision-induced dissociation MS/MS conditions and use in structural determination. Analytical Chemistry 2007; 79: 9022.
    • (2007) Analytical Chemistry , vol.79 , pp. 9022
    • Suzuki, K.1    Daikoku, S.2    Ako, T.3    Kurimoto, A.4    Ohtake, A.5    Shioiri, Y.6    Sarkar, S.K.7    Kanie, O.8
  • 37
    • 0002603882 scopus 로고
    • Cyclization of N-halogenated amines (The Hofmann-Löffler reaction)
    • Wolff ME. Cyclization of N-halogenated amines (The Hofmann-Löffler reaction). Chemical Reviews 1963; 63: 55.
    • (1963) Chemical Reviews , vol.63 , pp. 55
    • Wolff, M.E.1
  • 38
    • 30344433729 scopus 로고    scopus 로고
    • Intramolecular hydrogen bonding and hydrogen atom abstraction in gas-phase aliphatic amine radical cations
    • Hammerum S, Nielsen CB. Intramolecular hydrogen bonding and hydrogen atom abstraction in gas-phase aliphatic amine radical cations. Journal of Physical Chemistry A 2005; 109: 12046.
    • (2005) Journal of Physical Chemistry A , vol.109 , pp. 12046
    • Hammerum, S.1    Nielsen, C.B.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.