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Volumn 9, Issue 1, 1998, Pages 126-131

A new method for the synthesis of neoglycopeptides

Author keywords

[No Author keywords available]

Indexed keywords

ACETYLATION; CARBOHYDRATES;

EID: 0031983172     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc9700998     Document Type: Article
Times cited : (5)

References (29)
  • 5
    • 85069035566 scopus 로고
    • Solid-phase synthesis and conformational studies of glycosylated derivatives of helper-T-cell immunogenic peptides from hen-egg lysozyme
    • Elofsson, M., Roy, S., Walse, B., and Kihlberg, J. (1993) Solid-phase synthesis and conformational studies of glycosylated derivatives of helper-T-cell immunogenic peptides from hen-egg lysozyme. Carbohydr. Chem. 240, 89-103.
    • (1993) Carbohydr. Chem. , vol.240 , pp. 89-103
    • Elofsson, M.1    Roy, S.2    Walse, B.3    Kihlberg, J.4
  • 6
    • 0020197028 scopus 로고
    • High-performance liquid chromatography analysis in the synthesis, characterization, and reactions of neoglycopeptides
    • Morehead, H., McKay, P., and Wetzel, R. (1982) High-performance liquid chromatography analysis in the synthesis, characterization, and reactions of neoglycopeptides. Anal. Chem. 126, 29-36.
    • (1982) Anal. Chem. , vol.126 , pp. 29-36
    • Morehead, H.1    McKay, P.2    Wetzel, R.3
  • 7
    • 0025289980 scopus 로고
    • Synthesis of the N-glycopeptide partial sequence A1-A12 of the b-Chain og glycosylated haemoglobin HbA1c. A new approach to Amadori N-glycopeptides
    • Forrow, N. J., and Batchelor, M. J. (1990) Synthesis of the N-glycopeptide partial sequence A1-A12 of the b-Chain og glycosylated haemoglobin HbA1c. A new approach to Amadori N-glycopeptides. Tetrahedron Lett. 31, 3493-3495.
    • (1990) Tetrahedron Lett. , vol.31 , pp. 3493-3495
    • Forrow, N.J.1    Batchelor, M.J.2
  • 9
    • 85069022765 scopus 로고    scopus 로고
    • Solid phase coupling of unprotected reducing carbohydrates to the N-terminus of peptides
    • (R. Epton, Ed.) Mayflower, Andover, England (in press)
    • Boas, U., Heegaard, P., and Jakobsen, M. H. (1996) Solid phase coupling of unprotected reducing carbohydrates to the N-terminus of peptides. In Innovations and Perspectives in Solid Phase Synthesis (R. Epton, Ed.) Mayflower, Andover, England (in press).
    • (1996) Innovations and Perspectives in Solid Phase Synthesis
    • Boas, U.1    Heegaard, P.2    Jakobsen, M.H.3
  • 10
    • 21144461155 scopus 로고
    • Immobilization of reducing oligosacchararides to matrices by a glycosylamide linkage
    • Blomberg, L., Wieslander, J., and Norberg, T. (1993) Immobilization of reducing oligosacchararides to matrices by a glycosylamide linkage. J. Carbohydr. Chem. 12, 265-276.
    • (1993) J. Carbohydr. Chem. , vol.12 , pp. 265-276
    • Blomberg, L.1    Wieslander, J.2    Norberg, T.3
  • 11
    • 0026951967 scopus 로고
    • An effective method for the synthesis of neoglycoproteins and neogangliosides by use of reductively aminated sulfhydryl-containing carbohydrate conjugates
    • Schneller, M., and Geiger, R. E. (1992) An effective method for the synthesis of neoglycoproteins and neogangliosides by use of reductively aminated sulfhydryl-containing carbohydrate conjugates. Biol. Chem. Hoppe-Seyler 373, 1095-1104.
    • (1992) Biol. Chem. Hoppe-Seyler , vol.373 , pp. 1095-1104
    • Schneller, M.1    Geiger, R.E.2
  • 12
    • 0016906049 scopus 로고
    • Enzyme coupled immunoassay of insulin using a novel coupling reagent
    • Kitagawa, T., and Aikawa, T. (1976) Enzyme coupled immunoassay of insulin using a novel coupling reagent. J. Biochem. 76, 233-236.
    • (1976) J. Biochem. , vol.76 , pp. 233-236
    • Kitagawa, T.1    Aikawa, T.2
  • 13
    • 0025153687 scopus 로고
    • Recent advances in solid-phase peptide synthesis and preparation of antibodies to synthetic peptides
    • Plaué, S., Muller, S., Briand, J. P., and van Regenmortel, M. V. H. (1990) Recent advances in solid-phase peptide synthesis and preparation of antibodies to synthetic peptides. Biologicals 18, 147-157.
    • (1990) Biologicals , vol.18 , pp. 147-157
    • Plaué, S.1    Muller, S.2    Briand, J.P.3    Van Regenmortel, M.V.H.4
  • 14
    • 0029045908 scopus 로고
    • Maleimide-mediated proteincojugates of a nucleoside triphosphate gamma-S and an internucleotide phosphorothioate
    • Karim, A. S., Johansson, C. S., and Weltman, J. K. (1995) Maleimide-mediated proteincojugates of a nucleoside triphosphate gamma-S and an internucleotide phosphorothioate. Nucleic Acids Res. 23, 2037-2040.
    • (1995) Nucleic Acids Res. , vol.23 , pp. 2037-2040
    • Karim, A.S.1    Johansson, C.S.2    Weltman, J.K.3
  • 16
    • 0026461022 scopus 로고
    • A novel mild, specific and indirect maleimido-based radiolabeling method. Radiolabeling of analogs derived from parathyroid hormone (PTH) and PTH-ralated protein (PTHrP)
    • Chorev, M., Caulfield, M. P., Roubini, E., McKee, R. L., Gibbons, S. W., Leu, C.T., Levy, J. J., and Rosenblatt, M. (1992) A novel mild, specific and indirect maleimido-based radiolabeling method. Radiolabeling of analogs derived from parathyroid hormone (PTH) and PTH-ralated protein (PTHrP). Int. J. Pept. Protein Res. 40, 445-455.
    • (1992) Int. J. Pept. Protein Res. , vol.40 , pp. 445-455
    • Chorev, M.1    Caulfield, M.P.2    Roubini, E.3    McKee, R.L.4    Gibbons, S.W.5    Leu, C.T.6    Levy, J.J.7    Rosenblatt, M.8
  • 17
    • 0023181152 scopus 로고
    • Studies on Immunoassays of Peptide Factors V. Synthesis of cholecystokinin-58-1-11/Iso-1-cytochrorne c conjugate
    • Moroder, L., Tzougraki, C., Göhring, W., Mourier, G., Musiol, H.-J., and Wünsch, E. (1987) Studies on Immunoassays of Peptide Factors V. Synthesis of cholecystokinin-58-[1-11/Iso-1-cytochrorne c conjugate. Biol. Chem. Hoppe-Seyler 368, 855-861.
    • (1987) Biol. Chem. Hoppe-Seyler , vol.368 , pp. 855-861
    • Moroder, L.1    Tzougraki, C.2    Göhring, W.3    Mourier, G.4    Musiol, H.-J.5    Wünsch, E.6
  • 18
    • 0003834870 scopus 로고
    • Principle and practice of solid-phase peptide synthesis
    • (G. A. Grant, Ed.) W. H. Freeman and Co., New York
    • Fields, G. B., Tian, Z., and Barany, G. (1992) Principle and practice of solid-phase peptide synthesis. In Synthetic Peptides: A User's Guide (G. A. Grant, Ed.) pp 77-183, W. H. Freeman and Co., New York.
    • (1992) Synthetic Peptides: A User's Guide , pp. 77-183
    • Fields, G.B.1    Tian, Z.2    Barany, G.3
  • 19
    • 0027111692 scopus 로고
    • Fmoc-protected, glycosylated asparagines potentially useful as reagents in the solid-phase synthesis of N-glycopeptides
    • Urge, L., Otvos, L., Jr., Lang, E., Wroblewski, K., Laczko, I., and Hollosi, M. (1992) Fmoc-protected, glycosylated asparagines potentially useful as reagents in the solid-phase synthesis of N-glycopeptides. Carbohydr. Res. 235, 83-93.
    • (1992) Carbohydr. Res. , vol.235 , pp. 83-93
    • Urge, L.1    Otvos L., Jr.2    Lang, E.3    Wroblewski, K.4    Laczko, I.5    Hollosi, M.6
  • 20
    • 45249127652 scopus 로고
    • Trialkylsilanes as scavengers for the trifluoroacetic acid deblocking of protecting groups in peptide synthesis
    • Pearson, D. A., Blanchette, M., Baker, M. L., and Guidon, C. A. (1989) Trialkylsilanes as scavengers for the trifluoroacetic acid deblocking of protecting groups in peptide synthesis. Tetrahedron Lett. 30, 2739-2742.
    • (1989) Tetrahedron Lett. , vol.30 , pp. 2739-2742
    • Pearson, D.A.1    Blanchette, M.2    Baker, M.L.3    Guidon, C.A.4
  • 21
    • 0026414020 scopus 로고
    • Application of n-pentenyl glycosides in the regio- and stereo-controlled synthesis of α-Linked N-glycopeptides
    • Ratcliffe, A. J., Konradson, P., and Fraser-Reid, B. (1991) Application of n-pentenyl glycosides in the regio-and stereo-controlled synthesis of α-Linked N-glycopeptides. Carbohydr. Res. 216, 323-335.
    • (1991) Carbohydr. Res. , vol.216 , pp. 323-335
    • Ratcliffe, A.J.1    Konradson, P.2    Fraser-Reid, B.3
  • 22
    • 0016849770 scopus 로고
    • Preparation of some properties of maleimido acids and maleoyl derivatives of peptides
    • Keller, O., and Rudinger, J. (1975) Preparation of some properties of maleimido acids and maleoyl derivatives of peptides. Helv. Chim. Acta 58, 531-541.
    • (1975) Helv. Chim. Acta , vol.58 , pp. 531-541
    • Keller, O.1    Rudinger, J.2
  • 23
    • 0030250618 scopus 로고    scopus 로고
    • Introduction of the maleimide function onto resin-bound peptides: A simple high-yield process useful for discriminating among several lysines
    • Marburg, S., Neckers, A. C., and Griffin, P. G. (1996) Introduction of the maleimide function onto resin-bound peptides: A simple high-yield process useful for discriminating among several lysines. Bioconjugate Chem. 7, 612-616.
    • (1996) Bioconjugate Chem. , vol.7 , pp. 612-616
    • Marburg, S.1    Neckers, A.C.2    Griffin, P.G.3
  • 26
    • 85069029155 scopus 로고
    • Direct solid phase synthesis of N-maleoyl peptides
    • (R. Epton, Ed.) Mayflower, Andover, England
    • Jensen, S. P., and Jakobsen, M. H. (1994). Direct solid phase synthesis of N-maleoyl peptides. In Innovations and Perspectives in Solid Phase Synthesis (R. Epton, Ed.) pp 563-566, Mayflower, Andover, England.
    • (1994) Innovations and Perspectives in Solid Phase Synthesis , pp. 563-566
    • Jensen, S.P.1    Jakobsen, M.H.2
  • 27
    • 0027529269 scopus 로고
    • ∈-Nvoc-lysine and use in the preparation of selectively functionalized peptides
    • ∈-Nvoc-lysine and use in the preparation of selectively functionalized peptides. Bioorg. Med. Chem. Lett. 3, 707-710.
    • (1993) Bioorg. Med. Chem. Lett. , vol.3 , pp. 707-710
    • Rusiecki, V.K.1    Warne, S.A.2
  • 28
    • 0027654768 scopus 로고
    • Synthesis of dextrane derivatives with thiol-specific reactive groups for the preparation of dextran-protein conjugates
    • Herman, S., Persijn, G., Vandekerckhove, J., and Schacht, E. (1993) Synthesis of dextrane derivatives with thiol-specific reactive groups for the preparation of dextran-protein conjugates. Bioconjugate Chem. 4, 402-405.
    • (1993) Bioconjugate Chem. , vol.4 , pp. 402-405
    • Herman, S.1    Persijn, G.2    Vandekerckhove, J.3    Schacht, E.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.