메뉴 건너뛰기




Volumn 14, Issue 9, 2013, Pages 2973-2983

Synthetic glycopolypeptides as biomimetic analogues of natural glycoproteins

Author keywords

[No Author keywords available]

Indexed keywords

CELLULAR FUNCTION; CHEMICAL ROUTES; POLYMERIC STRUCTURES; PROTEIN GLYCOSYLATION; SCIENCE APPLICATIONS;

EID: 84883808425     PISSN: 15257797     EISSN: 15264602     Source Type: Journal    
DOI: 10.1021/bm4008088     Document Type: Review
Times cited : (99)

References (109)
  • 1
    • 0035937499 scopus 로고    scopus 로고
    • Chemical glycobiology
    • Bertozzi, C. R.; Kiessling, L. L. Chemical glycobiology Science 2001, 291, 2357-2364
    • (2001) Science , vol.291 , pp. 2357-2364
    • Bertozzi, C.R.1    Kiessling, L.L.2
  • 2
    • 0035937463 scopus 로고    scopus 로고
    • Towards automated synthesis of oligosaccharides and glycoproteins
    • Sears, P.; Wong, C. H. Towards automated synthesis of oligosaccharides and glycoproteins Science 2001, 291, 2344-2350
    • (2001) Science , vol.291 , pp. 2344-2350
    • Sears, P.1    Wong, C.H.2
  • 4
    • 0035937505 scopus 로고    scopus 로고
    • Intracellular functions of N-linked glycans
    • Helenius, A.; Aebi, M. Intracellular functions of N-linked glycans Science 2001, 291, 2364-2369
    • (2001) Science , vol.291 , pp. 2364-2369
    • Helenius, A.1    Aebi, M.2
  • 5
    • 84855919835 scopus 로고    scopus 로고
    • Recent advances in the synthesis of new glycopeptide antibiotics
    • Ashford, P. A.; Bew, S. P. Recent advances in the synthesis of new glycopeptide antibiotics Chem. Soc. Rev. 2012, 41, 957-978
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 957-978
    • Ashford, P.A.1    Bew, S.P.2
  • 6
    • 14544269999 scopus 로고    scopus 로고
    • Synthetic glycopeptidesand glycoproteins as tools for biology
    • Pratt, M. A.; Bertozzi, C. R. Synthetic glycopeptidesand glycoproteins as tools for biology Chem. Soc. Rev. 2005, 34, 58-68
    • (2005) Chem. Soc. Rev. , vol.34 , pp. 58-68
    • Pratt, M.A.1    Bertozzi, C.R.2
  • 7
    • 1642434197 scopus 로고    scopus 로고
    • Mimicking posttranslational modifications of proteins
    • Davis, B. G. Mimicking posttranslational modifications of proteins Science 2004, 303, 480-482
    • (2004) Science , vol.303 , pp. 480-482
    • Davis, B.G.1
  • 11
    • 84863393830 scopus 로고    scopus 로고
    • Synthesis and polypeptides by ring-opening polymerization of α-amino acid N -carboxyanhydrides
    • Cheng, J.; Deming, T. J. Synthesis and polypeptides by ring-opening polymerization of α-amino acid N -carboxyanhydrides Top. Curr. Chem. 2012, 310, 1-26
    • (2012) Top. Curr. Chem. , vol.310 , pp. 1-26
    • Cheng, J.1    Deming, T.J.2
  • 12
    • 55049090701 scopus 로고    scopus 로고
    • Polymer "clicking" by CuAAC reactions
    • Meldal, M. Polymer "clicking" by CuAAC reactions Macromol. Rapid Commun. 2008, 29, 1016-1051
    • (2008) Macromol. Rapid Commun. , vol.29 , pp. 1016-1051
    • Meldal, M.1
  • 13
    • 70349769688 scopus 로고    scopus 로고
    • Click chemistry beyond metal-catalyzed cycloaddition
    • Becer, C. R.; Hoogenboom, R.; Schubert, U. S. Click chemistry beyond metal-catalyzed cycloaddition Angew. Chem., Int. Ed. 2009, 48 (27) 4900-4908
    • (2009) Angew. Chem., Int. Ed. , vol.48 , Issue.27 , pp. 4900-4908
    • Becer, C.R.1    Hoogenboom, R.2    Schubert, U.S.3
  • 16
    • 0033038265 scopus 로고    scopus 로고
    • Genetic optimization of recombinant glycoprotein production by mammalian cells
    • Fussenegger, M.; Bailey, J. E.; Hauser, H.; Mueller, P. P. Genetic optimization of recombinant glycoprotein production by mammalian cells Trends Biotechnol. 1999, 17 (1) 35-42
    • (1999) Trends Biotechnol. , vol.17 , Issue.1 , pp. 35-42
    • Fussenegger, M.1    Bailey, J.E.2    Hauser, H.3    Mueller, P.P.4
  • 19
    • 79957475745 scopus 로고    scopus 로고
    • Chemistry and glycobiology
    • Wu, C. Y.; Wong, C. H. Chemistry and glycobiology Chem. Commun. 2011, 47, 6201-6207
    • (2011) Chem. Commun. , vol.47 , pp. 6201-6207
    • Wu, C.Y.1    Wong, C.H.2
  • 20
    • 84883778857 scopus 로고    scopus 로고
    • Total synthesis of erythropoietin through the development and exploitation of enabling synthetic technologies
    • Payne, R. J. Total synthesis of erythropoietin through the development and exploitation of enabling synthetic technologies Angew. Chem., Int. Ed. 2012, 51, 2-5
    • (2012) Angew. Chem., Int. Ed. , vol.51 , pp. 2-5
    • Payne, R.J.1
  • 23
    • 34547908618 scopus 로고    scopus 로고
    • Synthesis and application of glycopeptide and glycoprotein mimetics
    • Specker, D.; Wittmann, V. Synthesis and application of glycopeptide and glycoprotein mimetics Top. Curr. Chem. 2007, 267, 65-107
    • (2007) Top. Curr. Chem. , vol.267 , pp. 65-107
    • Specker, D.1    Wittmann, V.2
  • 24
    • 0034504913 scopus 로고    scopus 로고
    • Synthesis of glycopeptides containing carbohydrate and peptide recognition motifs
    • Herzner, H.; Reipen, T.; Schultz, M.; Kunz, H. Synthesis of glycopeptides containing carbohydrate and peptide recognition motifs Chem. Rev. 2000, 100, 4495-4537
    • (2000) Chem. Rev. , vol.100 , pp. 4495-4537
    • Herzner, H.1    Reipen, T.2    Schultz, M.3    Kunz, H.4
  • 25
    • 84985598642 scopus 로고
    • Synthesis of glycopeptides, partial structures of biological recognition components
    • Kunz, H. Synthesis of glycopeptides, partial structures of biological recognition components Angew. Chem., Int. Ed. 1987, 26 (4) 294-308
    • (1987) Angew. Chem., Int. Ed. , vol.26 , Issue.4 , pp. 294-308
    • Kunz, H.1
  • 26
    • 72149096309 scopus 로고    scopus 로고
    • Advances in chemical ligation strategies for the synthesis of glycopeptides and glycoproteins
    • Payne, R. J.; Wong, C. H. Advances in chemical ligation strategies for the synthesis of glycopeptides and glycoproteins Chem. Commun. 2010, 46, 21-43
    • (2010) Chem. Commun. , vol.46 , pp. 21-43
    • Payne, R.J.1    Wong, C.H.2
  • 28
    • 0035961527 scopus 로고    scopus 로고
    • Chemoselective elaboration of O-linked glycopeptide mimetics by alkylation of 3-thiogalnac
    • Marcaurelle, L. A.; Bertozzi, C. R. Chemoselective elaboration of O-linked glycopeptide mimetics by alkylation of 3-thiogalnac J. Am. Chem. Soc. 2001, 123, 1587-1595
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 1587-1595
    • Marcaurelle, L.A.1    Bertozzi, C.R.2
  • 29
    • 0034899741 scopus 로고    scopus 로고
    • Fully convergent solid phase synthesis of antifreeze glycoprotein analogues
    • Eniade, A.; Ben, R. N. Fully convergent solid phase synthesis of antifreeze glycoprotein analogues Biomacromolecules 2001, 2, 557-561
    • (2001) Biomacromolecules , vol.2 , pp. 557-561
    • Eniade, A.1    Ben, R.N.2
  • 30
    • 33644589005 scopus 로고    scopus 로고
    • Aggregation of antifreeze glycoprotein fraction 8 and its effect on antifreeze activity
    • Bouvet, V. R.; Lorello, G. R.; Ben, R. N. Aggregation of antifreeze glycoprotein fraction 8 and its effect on antifreeze activity Biomacromolecules 2006, 2006 (7) 565-571
    • (2006) Biomacromolecules , vol.2006 , Issue.7 , pp. 565-571
    • Bouvet, V.R.1    Lorello, G.R.2    Ben, R.N.3
  • 35
    • 70349999667 scopus 로고    scopus 로고
    • Recent departures in the synthesis of peptides and glycopeptides
    • Kan, C.; Danishefsky, S. J. Recent departures in the synthesis of peptides and glycopeptides Tetrahedron 2009, 65, 9047-9065
    • (2009) Tetrahedron , vol.65 , pp. 9047-9065
    • Kan, C.1    Danishefsky, S.J.2
  • 43
    • 37349094422 scopus 로고    scopus 로고
    • Free-radical-based, specific desulfurization of cysteine: A powerful advance in the synthesis of polypeptides and glycopolypeptides
    • Wan, Q.; Danishefsky, S. J. Free-radical-based, specific desulfurization of cysteine: a powerful advance in the synthesis of polypeptides and glycopolypeptides Angew. Chem., Int. Ed. 2007, 46, 9248-9252
    • (2007) Angew. Chem., Int. Ed. , vol.46 , pp. 9248-9252
    • Wan, Q.1    Danishefsky, S.J.2
  • 45
    • 34547330140 scopus 로고    scopus 로고
    • Chemoenzymatic approaches to glycoprotein synthesis
    • Bennett, C. S.; Wong, C. H. Chemoenzymatic approaches to glycoprotein synthesis Chem. Soc. Rev. 2007, 36, 1227-1238
    • (2007) Chem. Soc. Rev. , vol.36 , pp. 1227-1238
    • Bennett, C.S.1    Wong, C.H.2
  • 47
    • 79954613973 scopus 로고    scopus 로고
    • Biohybrid block copolymers: Towards functional micelles and vesicles
    • Fuks, G.; Mayap Talom, R.; Gauffre, F. Biohybrid block copolymers: Towards functional micelles and vesicles Chem. Soc. Rev. 2011, 40, 2475-2493
    • (2011) Chem. Soc. Rev. , vol.40 , pp. 2475-2493
    • Fuks, G.1    Mayap Talom, R.2    Gauffre, F.3
  • 48
    • 84866117794 scopus 로고    scopus 로고
    • Self-assembly of block copolymers
    • Mai, Y.; Eisenberg, A. Self-assembly of block copolymers Chem. Soc. Rev. 2012, 41, 5969-5985
    • (2012) Chem. Soc. Rev. , vol.41 , pp. 5969-5985
    • Mai, Y.1    Eisenberg, A.2
  • 50
    • 84858763063 scopus 로고    scopus 로고
    • Towards bioactive nanovehicles based on protein polymers
    • Garanger, E.; Lecommandoux, S. Towards bioactive nanovehicles based on protein polymers Angew. Chem., Int. Ed. 2012, 51 (13) 3060-3062
    • (2012) Angew. Chem., Int. Ed. , vol.51 , Issue.13 , pp. 3060-3062
    • Garanger, E.1    Lecommandoux, S.2
  • 51
    • 78649716734 scopus 로고    scopus 로고
    • Synthesis of glycopolymers and their multivalent recognitions with lectins
    • Ting, S. R. S.; Chen, G.; Stenzel, M. H. Synthesis of glycopolymers and their multivalent recognitions with lectins Polym. Chem. 2010, 1, 1392-1412
    • (2010) Polym. Chem. , vol.1 , pp. 1392-1412
    • Ting, S.R.S.1    Chen, G.2    Stenzel, M.H.3
  • 58
    • 73249151312 scopus 로고    scopus 로고
    • Synthesis of well-defined polypeptide-based materials via the ring-opening polymerization of α-amino acid N -carboxyanhydrides
    • Hadjichristidis, N.; Iatrou, H.; Pitsikalis, M.; Sakellariou, G. Synthesis of well-defined polypeptide-based materials via the ring-opening polymerization of α-amino acid N -carboxyanhydrides Chem. Rev. 2009, 109, 5528-5578
    • (2009) Chem. Rev. , vol.109 , pp. 5528-5578
    • Hadjichristidis, N.1    Iatrou, H.2    Pitsikalis, M.3    Sakellariou, G.4
  • 59
    • 0031440842 scopus 로고    scopus 로고
    • Facile synthesis of block copolypeptides of defined architecture
    • Deming, T. J. Facile synthesis of block copolypeptides of defined architecture Nature 1997, 390, 386-389
    • (1997) Nature , vol.390 , pp. 386-389
    • Deming, T.J.1
  • 60
    • 68749100661 scopus 로고    scopus 로고
    • Self-assembly of polypeptide-based block copolymer amphiphiles
    • Carlsen, A.; Lecommandoux, S. Self-assembly of polypeptide-based block copolymer amphiphiles Curr. Opin. Colloid Interface Sci. 2009, 14, 329-339
    • (2009) Curr. Opin. Colloid Interface Sci. , vol.14 , pp. 329-339
    • Carlsen, A.1    Lecommandoux, S.2
  • 61
    • 70449397517 scopus 로고    scopus 로고
    • Peptide-synthetic polymer conjugates
    • Klok, H. A. Peptide-synthetic polymer conjugates Macromolecules 2009, 42, 7990-8000
    • (2009) Macromolecules , vol.42 , pp. 7990-8000
    • Klok, H.A.1
  • 62
    • 84878774848 scopus 로고    scopus 로고
    • Stimuli responsive synthetic polypeptides derived from N -carboxyanhydride (NCA) polymerisation
    • 10.1039/C3CS60063G
    • Huang, J.; Heise, A. Stimuli responsive synthetic polypeptides derived from N -carboxyanhydride (NCA) polymerisation Chem. Soc. Rev. 2013, 10.1039/C3CS60063G
    • (2013) Chem. Soc. Rev.
    • Huang, J.1    Heise, A.2
  • 63
    • 0344010977 scopus 로고    scopus 로고
    • Synthesis of nearly monodisperse polystyrene-polypeptide block copolymers via polymerization of NCA
    • Dimitrov, I.; Schlaad, H. Synthesis of nearly monodisperse polystyrene-polypeptide block copolymers via polymerization of NCA Chem. Commun. 2003, 2944-2945
    • (2003) Chem. Commun. , pp. 2944-2945
    • Dimitrov, I.1    Schlaad, H.2
  • 66
    • 77958510703 scopus 로고    scopus 로고
    • Glycopolypeptides via living polymerization of glycosylated- l -lysine N -carboxyanhydrides
    • Kramer, J. R.; Deming, T. J. Glycopolypeptides via living polymerization of glycosylated- l -lysine N -carboxyanhydrides J. Am. Chem. Soc. 2010, 132, 15068-15071
    • (2010) J. Am. Chem. Soc. , vol.132 , pp. 15068-15071
    • Kramer, J.R.1    Deming, T.J.2
  • 67
    • 0028195162 scopus 로고
    • Glycopeptide synthesis by NCA method ROP of sugar substituted NCA
    • Aoi, K.; Tsutsumiuchi, K.; Okada, M. Glycopeptide synthesis by NCA method ROP of sugar substituted NCA Macromolecules 1994, 27, 875-877
    • (1994) Macromolecules , vol.27 , pp. 875-877
    • Aoi, K.1    Tsutsumiuchi, K.2    Okada, M.3
  • 68
    • 84857854947 scopus 로고    scopus 로고
    • Glycopolypeptides with a redox-triggered helix-to-coil transition
    • Kramer, J. R.; Deming, T. J. Glycopolypeptides with a redox-triggered helix-to-coil transition J. Am. Chem. Soc. 2012, 134, 4112-4115
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 4112-4115
    • Kramer, J.R.1    Deming, T.J.2
  • 70
    • 84860868858 scopus 로고    scopus 로고
    • Multiple topologies from glycopolypeptide-dendron conjugate self-assembly: Nanorods, micelles and organogels
    • Pati, D.; Kalva, N.; Das, S.; Kumaraswamy, G.; Gupta, S. S.; Ambade, A. V. Multiple topologies from glycopolypeptide-dendron conjugate self-assembly: Nanorods, micelles and organogels J. Am. Chem. Soc. 2012, 134, 7796-7802
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 7796-7802
    • Pati, D.1    Kalva, N.2    Das, S.3    Kumaraswamy, G.4    Gupta, S.S.5    Ambade, A.V.6
  • 71
    • 84861175987 scopus 로고    scopus 로고
    • Controlled synthesis of O -glycopolypeptide polymers and their molecular recognition by lectins
    • Pati, D.; Shaikh, A. Y.; Das, S.; Nareddy, P. K.; Swamy, M. J.; Hotha, S.; Gupta, S. S. Controlled synthesis of O -glycopolypeptide polymers and their molecular recognition by lectins Biomacromolecules 2012, 13, 1287-1295
    • (2012) Biomacromolecules , vol.13 , pp. 1287-1295
    • Pati, D.1    Shaikh, A.Y.2    Das, S.3    Nareddy, P.K.4    Swamy, M.J.5    Hotha, S.6    Gupta, S.S.7
  • 72
    • 79952742893 scopus 로고    scopus 로고
    • Synthesis of glycopolypeptides by the ring opening polymerization of O -glycosylated-α-amino acid N -carboxyanhydride (NCA)
    • Pati, D.; Shaikh, A. Y.; Hotha, S.; Gupta, S. S. Synthesis of glycopolypeptides by the ring opening polymerization of O -glycosylated-α- amino acid N -carboxyanhydride (NCA) Polym. Chem. 2011, 2, 805-811
    • (2011) Polym. Chem. , vol.2 , pp. 805-811
    • Pati, D.1    Shaikh, A.Y.2    Hotha, S.3    Gupta, S.S.4
  • 73
    • 80052041782 scopus 로고    scopus 로고
    • Facile synthesis of unusual glycosyl carbamates and amino acid glycosides from propargyl 1,2-orthoesters as glycosyl donors
    • Shaikh, A. Y.; Sureshkumar, G.; Pati, D.; Gupta, S. S.; Hotha, S. Facile synthesis of unusual glycosyl carbamates and amino acid glycosides from propargyl 1,2-orthoesters as glycosyl donors Org. Biomol. Chem. 2011, 9, 5951-5959
    • (2011) Org. Biomol. Chem. , vol.9 , pp. 5951-5959
    • Shaikh, A.Y.1    Sureshkumar, G.2    Pati, D.3    Gupta, S.S.4    Hotha, S.5
  • 74
    • 84867068839 scopus 로고    scopus 로고
    • Poly-amido-saccharides: Synthesis via anionic polymerization of a β-lactam monomer
    • Dane, E. L.; Grinstaff, M. W. Poly-amido-saccharides: Synthesis via anionic polymerization of a β-lactam monomer J. Am. Chem. Soc. 2012, 134, 16255-16264
    • (2012) J. Am. Chem. Soc. , vol.134 , pp. 16255-16264
    • Dane, E.L.1    Grinstaff, M.W.2
  • 75
    • 77952766890 scopus 로고    scopus 로고
    • Facile control of the self-assembled structures of polylysines having pendent mannose groups via pH and surfactant
    • Wang, R.; Xu, N.; Du, F. S.; Li, Z. C. Facile control of the self-assembled structures of polylysines having pendent mannose groups via pH and surfactant Chem. Commun. 2010, 46, 3902-3904
    • (2010) Chem. Commun. , vol.46 , pp. 3902-3904
    • Wang, R.1    Xu, N.2    Du, F.S.3    Li, Z.C.4
  • 76
    • 38349077144 scopus 로고    scopus 로고
    • Preparation and evaluation of novel amphiphilic glycopeptide block copolymers as carriers for controlled drug release
    • Tian, Z.; Wang, M.; Zhang, A. Y.; Feng, Z. G. Preparation and evaluation of novel amphiphilic glycopeptide block copolymers as carriers for controlled drug release Polymer 2008, 49, 446-454
    • (2008) Polymer , vol.49 , pp. 446-454
    • Tian, Z.1    Wang, M.2    Zhang, A.Y.3    Feng, Z.G.4
  • 77
    • 0032211199 scopus 로고    scopus 로고
    • Analysis of specific interactions of synthetic glycopolypeptides carrying N -acetyllactosamine and related coumpounds with lectins
    • Zeng, X.; Murata, T.; Kawagishi, H.; Usui, T.; Kobayashi, K. Analysis of specific interactions of synthetic glycopolypeptides carrying N -acetyllactosamine and related coumpounds with lectins Carbohyd. Res. 1998, 312, 209-217
    • (1998) Carbohyd. Res. , vol.312 , pp. 209-217
    • Zeng, X.1    Murata, T.2    Kawagishi, H.3    Usui, T.4    Kobayashi, K.5
  • 78
    • 0032084497 scopus 로고    scopus 로고
    • Synthesis of artificial N -glycopolypeptides carrying N -acetyllactosamine and related coumpounds and their specific interactions with lectins
    • Zeng, X.; Murata, T.; Kawagishi, H.; Usui, T.; Kobayashi, K. Synthesis of artificial N -glycopolypeptides carrying N -acetyllactosamine and related coumpounds and their specific interactions with lectins Biosci. Biotechnol. Biochem. 1998, 62 (6) 1171-1178
    • (1998) Biosci. Biotechnol. Biochem. , vol.62 , Issue.6 , pp. 1171-1178
    • Zeng, X.1    Murata, T.2    Kawagishi, H.3    Usui, T.4    Kobayashi, K.5
  • 79
    • 0030843796 scopus 로고    scopus 로고
    • Artificial glycopolypeptides conjugates: Simple synthesis of lactose- and N, N ′-diacetylchitobiose-substituted poly(l -glutamic acid)s through N -β-glycoside linkages and their interaction with lectins
    • Kobayashi, K.; Tawada, E.; Akaike, T.; Usui, T. Artificial glycopolypeptides conjugates: Simple synthesis of lactose- and N, N ′-diacetylchitobiose-substituted poly(l -glutamic acid)s through N -β-glycoside linkages and their interaction with lectins Biochim. Biophys. Acta 1997, 1336, 117-122
    • (1997) Biochim. Biophys. Acta , vol.1336 , pp. 117-122
    • Kobayashi, K.1    Tawada, E.2    Akaike, T.3    Usui, T.4
  • 81
    • 84862152432 scopus 로고    scopus 로고
    • Preparation of multifunctional and multireactive polypeptides via methionine alkylation
    • Kramer, J. R.; Deming, T. J. Preparation of multifunctional and multireactive polypeptides via methionine alkylation Biomacromolecules 2012, 13, 1719-1723
    • (2012) Biomacromolecules , vol.13 , pp. 1719-1723
    • Kramer, J.R.1    Deming, T.J.2
  • 86
    • 35348814929 scopus 로고    scopus 로고
    • Effects of saccharide spacing and chain extension on toxin inhibition by glycopolypeptides of well-defined architecture
    • Polizzotti, B. D.; Maheshwari, R.; Vinkenborg, J.; Kiick, K. L. Effects of saccharide spacing and chain extension on toxin inhibition by glycopolypeptides of well-defined architecture Macromolecules 2007, 40, 7103-7110
    • (2007) Macromolecules , vol.40 , pp. 7103-7110
    • Polizzotti, B.D.1    Maheshwari, R.2    Vinkenborg, J.3    Kiick, K.L.4
  • 87
    • 80855164568 scopus 로고    scopus 로고
    • Architecture effects on l -selectin shedding induced by polypeptide-based multivalent ligand
    • Liu, S.; Kiick, K. L. Architecture effects on l -selectin shedding induced by polypeptide-based multivalent ligand Polym. Chem. 2011, 2, 1513-1522
    • (2011) Polym. Chem. , vol.2 , pp. 1513-1522
    • Liu, S.1    Kiick, K.L.2
  • 89
    • 77955335291 scopus 로고    scopus 로고
    • Hydrolytically stable bioactive synthetic glycopolypeptide homo and copolymers by combination of NCA polymerization and click reaction
    • Huang, J.; Habraken, G.; Audouin, F.; Heise, A. Hydrolytically stable bioactive synthetic glycopolypeptide homo and copolymers by combination of NCA polymerization and click reaction Macromolecules 2010, 43, 6050-6057
    • (2010) Macromolecules , vol.43 , pp. 6050-6057
    • Huang, J.1    Habraken, G.2    Audouin, F.3    Heise, A.4
  • 90
    • 77953015913 scopus 로고    scopus 로고
    • Facile synthesis of glycopolypeptides by combination of ring-opening polymerization of an alkyne-substituted N -carboxyanhydride and click "glycosylation"
    • Xiao, C.; Zhao, C.; He, P.; Tang, Z.; Chen, X.; Jing, X. Facile synthesis of glycopolypeptides by combination of ring-opening polymerization of an alkyne-substituted N -carboxyanhydride and click "glycosylation" Macromol. Rapid Commun. 2010, 31, 991-997
    • (2010) Macromol. Rapid Commun. , vol.31 , pp. 991-997
    • Xiao, C.1    Zhao, C.2    He, P.3    Tang, Z.4    Chen, X.5    Jing, X.6
  • 92
    • 84877987556 scopus 로고    scopus 로고
    • Soluble, clickable polypeptides from azide-containing NCA
    • Rhodes, A. J.; Deming, T. J. Soluble, clickable polypeptides from azide-containing NCA ACS Macro Lett. 2013, 2, 351-354
    • (2013) ACS Macro Lett. , vol.2 , pp. 351-354
    • Rhodes, A.J.1    Deming, T.J.2
  • 93
    • 84865522289 scopus 로고    scopus 로고
    • Synthesis and self-assembly of "tree-like" amphiphilic glycopolypeptides
    • Bonduelle, C.; Huang, J.; Ibarboure, E.; Heise, A.; Lecommandoux, S. Synthesis and self-assembly of "tree-like" amphiphilic glycopolypeptides Chem. Commun. 2012, 48, 8353-8355
    • (2012) Chem. Commun. , vol.48 , pp. 8353-8355
    • Bonduelle, C.1    Huang, J.2    Ibarboure, E.3    Heise, A.4    Lecommandoux, S.5
  • 94
    • 77952490504 scopus 로고    scopus 로고
    • Thiol-ene clickable polypeptides
    • Sun, J.; Schlaad, H. Thiol-ene clickable polypeptides Macromolecules 2010, 43, 4445-4448
    • (2010) Macromolecules , vol.43 , pp. 4445-4448
    • Sun, J.1    Schlaad, H.2
  • 100
    • 0031189814 scopus 로고    scopus 로고
    • Synthesis of polyoxazoline-glycopeptide block copolymers by ROP
    • Tsutsumiuchi, K.; Aoi, K.; Okada, M. Synthesis of polyoxazoline- glycopeptide block copolymers by ROP Macromolecules 1997, 30, 4013-4017
    • (1997) Macromolecules , vol.30 , pp. 4013-4017
    • Tsutsumiuchi, K.1    Aoi, K.2    Okada, M.3
  • 101
    • 0000645730 scopus 로고    scopus 로고
    • First synthesis of glycopeptide macromonomers
    • Aoi, K.; Tsutsumiuchi, K.; Aoki, E.; Okada, M. First synthesis of glycopeptide macromonomers Macromolecules 1996, 29, 4456-4458
    • (1996) Macromolecules , vol.29 , pp. 4456-4458
    • Aoi, K.1    Tsutsumiuchi, K.2    Aoki, E.3    Okada, M.4
  • 104
    • 33947410029 scopus 로고    scopus 로고
    • Bioinspired functional block copolymers
    • Börner, H. G.; Schlaad, H. Bioinspired functional block copolymers Soft Matter 2007, 3, 394-408
    • (2007) Soft Matter , vol.3 , pp. 394-408
    • Börner, H.G.1    Schlaad, H.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.